Comprehensive Hematology Panel

PLUSbpg-method Plus Analysis combines Sequence + Del/Dup (CNV) Analysis providing increased diagnostic yield in certain clinical conditions, where the underlying genetic defect may be detectable by either of the analysis methods. Results in 3–4 weeks. SEQbpg-method Our Sequence Analysis is based on a proprietary targeted sequencing method OS-Seq™ and offers panels targeted for genes associated with certain phenotypes. A standard way to analyze NGS data for finding the genetic cause for Mendelian disorders. Results in 3–4 weeks. DEL/DUPbpg-method Targeted Del/Dup (CNV) analysis is used to detect bigger disease causing deletions or duplications from the disease-associated genes. Results in 3–4 weeks.

Test code: HE0101

The Blueprint Genetics Comprehensive Hematology Panel is a 175 gene test for genetic diagnostics of patients with clinical suspicion of hereditary anemia, inherited bleeding disorder, inherited bone marrow failure syndrome or leukemia.

This panel offers comprehensive genetic diagnostics for a broad range of hematological disorders varying from bone marrow failure to specific disorders affecting different cell populations or factors involved in hemostasis. These include congenital defects in neutrophils, inherited disorders in platelets and platelet function and a broad spectrum of red blood cell disorders. This panel comprises all the subpanels under the Hematology category.

About Hematological Diseases

Inherited hematological diseases are a group of blood disorders with variable clinical presentation. Depending on the underlying defect and the affected hematological cell populations the symptoms can vary from bleeding disorders to severe anemia or may cause significant immunosuppression. Furthermore, the inherited defects in coagulopathy may also cause thrombophilia increasing the risk of thrombosis already during the childhood. All genetic defects presenting bone marrow failure lead to severe immunosuppression possibly necessitating stem cell transplantation as a curative choice of treatment. Patients with inherited bone marrow failure syndromes have a high risk of developing cancer, either leukemia or solid tumors. The role of genetic diagnostics in inherited hematological diseases is essential. Currently, accurate genetic diagnosis is necessary to confirm the diagnosis of certain hematological diseases and guide their optimal treatment.


Results in 3-4 weeks. We do not offer a maternal cell contamination (MCC) test at the moment. We offer prenatal testing only for cases where the maternal cell contamination studies (MCC) are done by a local genetic laboratory. Read more:

Genes in the Comprehensive Hematology Panel and their clinical significance
Gene Associated phenotypes Inheritance ClinVar HGMD
ABCA3 Interstitial lung disease, Surfactant metabolism dysfunction, pulmonary AD/AR 11 181
ABCB7 Anemia, sideroblastic, and spinocerebellar ataxia XL 9 6
ABCG5 Sitosterolemia AR 10 37
ABCG8 Sitosterolemia AR 11 38
ACTB* Baraitser-Winter syndrome AD 27 26
ACTN1 Bleeding disorder, platelet- AD 6 25
ADAMTS13 Schulman-Upshaw syndrome, Thrombotic thrombocytopenic purpura, familial AR 22 172
AK2 Reticular dysgenesis AR 14 17
ALAS2 Anemia, sideroblastic, Protoporphyria, erythropoietic XL 27 93
AMN Megaloblastic anemia-1, Norwegian AR 24 32
ANK1 Spherocytosis AD/AR 12 82
ANKRD26 Thrombocytopenia AD 5 19
AP3B1 Hermansky-Pudlak syndrome AR 14 23
ATM Breast cancer, Ataxia-Telangiectasia AD/AR 455 853
ATR Cutaneous telangiectasia and cancer syndrome, Seckel syndrome AD/AR 6 13
ATRX Carpenter-Waziri syndrome, Alpha-thalassemia/mental retardation syndrome, Holmes-Gang syndrome, Juberg-Marsidi syndrome, Smith-Fineman-Myers syndrome, Mental retardation-hypotonic facies syndrome XL 42 149
BLM Bloom syndrome AR 53 92
BLOC1S3 Hermansky-Pudlak syndrome AR 1 2
BLOC1S6 Hermansky-Pudlak syndrome AR 1 1
BRCA2 Fanconi anemia, Medulloblastoma, Glioma susceptibility, Pancreatic cancer, Wilms tumor, Breast-ovarian cancer, familial AD/AR 2514 1791
BRIP1 Fanconi anemia, Breast cancer AD/AR 87 87
C15ORF41 Congenital dyserythropoietic anemia AR 2
CDAN1 Anemia, dyserythropoietic congenital AR 10 43
CDKN2A Melanoma, familial, Melanoma-pancreatic cancer syndrome AD 37 217
CEBPA Acute myeloid leukemia, familial AD 12 9
CSF2RA* Surfactant metabolism dysfunction, pulmonary XL 2 14
CTC1 Cerebroretinal microangiopathy with calcifications and cysts AR 13 29
CTSC Periodontitis, juvenile, Haim-Munk syndrome, Papillon-Lefevre syndrome AR 15 91
CUBN* Megaloblastic anemia-1, Finnish AR 32 49
CXCR4 Warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome AD 4 14
CYCS* Thrombocytopenia AD 2 3
DKC1 Hoyeraal-Hreidarsson syndrome, Dyskeratosis congenita XL 45 69
DTNBP1 Hermansky-Pudlak syndrome AR 2 3
ELANE Neutropenia AD 30 213
EPB42 Spherocytosis AR 9 12
ERCC4 Fanconi anemia, Xeroderma pigmentosum AR 11 37
F2 Thrombophilia due to thrombin defect, Prothrombin deficiency, congenital AD/AR 14 66
F5 Factor V deficiency, Thrombophilia due to activated protein C resistance AD/AR 18 162
F7 Factor VII deficiency AR 23 304
F8* Hemophilia A XL 276 3074
F9 Hemophilia B, Warfarin sensitivity, Thrombophilia, due to factor IX defect XL 109 1260
F10 Factor X deficiency AR 15 147
F11 Factor XI deficiency AD/AR 35 250
F12 Angioedema AD/AR 5 53
F13A1 Factor XIIIA deficiency AR 20 165
FANCA Fanconi anemia AR 33 474
FANCB Fanconi anemia XL 7 14
FANCC Fanconi anemia AR 34 34
FANCD2* Fanconi anemia AR 10 49
FANCE Fanconi anemia AR 3 9
FANCF Fanconia anemia AR 6 8
FANCG Fanconi anemia AR 11 73
FANCI Fanconi anemia AR 8 27
FANCL Fanconi anemia AR 6 15
FANCM Fanconi anemia AR 1 13
FAS Autoimmune lymphoproliferative syndrome AD/AR 22 136
FGA Afibrinogenemia, congenital, Dysfibrinogenemia, congenital, Hypodysfibrinogenemia, congenital, Familial visceral amyloidosis AD/AR 9 140
FGB Afibrinogenemia, congenital, Dysfibrinogenemia, congenital, Hypodysfibrinogenemia, congenital AD/AR 6 88
FGG Afibrinogenemia, congenital, Hypodysfibrinogenemia, Dysfibrinogenemia, congenital, Hypodysfibrinogenemia, congenital AD/AR 5 127
FLNA Frontometaphyseal dysplasia, Osteodysplasty Melnick-Needles, Otopalatodigital syndrome type 1, Otopalatodigital syndrome type 2, Terminal osseous dysplasia with pigmentary defects XL 86 209
G6PC3 Neutropenia, severe congenital, Dursun syndrome AR 12 37
G6PD Glucose-6-phosphate dehydrogenase deficiency XL 36 214
GATA1 Anemia, without thrombocytopenia, Thrombocytopenia with beta-thalessemia,, Dyserythropoietic anemia with thrombocytopenia XL 16 14
GATA2 Myelodysplastic syndrome, Chronic neutropenia associated with monocytopenia, evolving to myelodysplasia and acute myeloid leukemia, Acute myeloid leukemia, Emberger syndrome, Immunodeficiency AD 19 76
GGCX Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency, Vitamin K-dependent clotting factors, combined deficiency AD/AR/Digenic 13 38
GP1BA Pseudo-von Willebrand disease, Bernard-Soulier syndrome AD/AR 6 70
GP1BB Giant platelet disorder, isolated, Bernard-Soulier syndrome AD/AR 5 48
GP9 Bernard-Soulier syndrome AR 6 39
GPI Hemolytic anemia, nonspherocytic due to glucose phosphate isomerase deficiency AD 10 37
GPR143 Nystagmus, congenital, Ocular albinism XL 14 128
GSS Glutathione synthetase deficiency AR 7 34
HAX1 Neutropenia, severe congenital AR 8 19
HBA1* Alpha-thalassemia (Hemoglobin Bart syndrome), Alpha-thalassemia (Hemoglobin H disease) AR/Digenic 8 197
HBA2* Alpha-thalassemia (Hemoglobin Bart syndrome), Alpha-thalassemia (Hemoglobin H disease) AR/Digenic 22 279
HBB Sickle cell disease, Thalassemia-beta, dominant inclusion body, Other Thalassemias/Hemoglobinopathies, Beta-thalassemia AD/AR/Digenic 175 835
HFE Hemochromatosis AR/Digenic 7 53
HOXA11 Radioulnar synostosis with amegakaryocytic thrombocytopenia AD 1 1
HPS1* Hermansky-Pudlak syndrome AR 26 41
HPS3 Hermansky-Pudlak syndrome AR 8 13
HPS4 Hermansky-Pudlak syndrome AR 14 15
HPS5 Hermansky-Pudlak syndrome AR 7 14
HPS6 Hermansky-Pudlak syndrome AR 9 24
HRAS Costello syndrome, Congenital myopathy with excess of muscle spindles AD 30 26
IFNGR2 Immunodeficiency AR 4 18
ITGA2 Fetal and neonatal alloimmune thrombocytopenia AD/AR 10
ITGA2B Glanzmann thrombasthenia AD/AR 17 210
ITGB3 Bleeding disorder, platelet-, Thrombocytopenia, neonatal alloimmune, Glanzmann thrombasthenia AD/AR 16 152
ITK Lymphoproliferative syndrome AR 3 10
JAGN1 Neutropenia, severe congenital AR 8 8
KLF1 Anemia, dyserythropoietic congenital, Blood group, Lutheran inhibitor AD/BG 16 63
KRAS* Noonan syndrome, Cardiofaciocutaneous syndrome AD 46 38
LMAN1 Combined factor V and VIII deficiency AR 5 37
LPIN2 Majeed syndrome AR 8 10
LYST Chediak-Higashi syndrome AR 45 78
MAGT1 Immunodeficiency, with magnesium defect, Epstein-Barr virus infection and neoplasia XL 4 10
MASTL Thrombocytopenia AD 1 3
MLH1 Muir-Torre syndrome, Endometrial cancer, Mismatch repair cancer syndrome, Colorectal cancer, hereditary nonpolyposis AD/AR 670 1084
MPL Thrombocythemia, Amegakaryocytic thrombocytopenia AD/AR 14 50
MSH2 Muir-Torre syndrome, Endometrial cancer, Colorectal cancer, hereditary nonpolyposis,, Mismatch repair cancer syndrome AD/AR 646 1089
MSH6 Endometrial cancer, Mismatch repair cancer syndrome, Colorectal cancer, hereditary nonpolyposis AD/AR 308 426
MTR Methylmalonic acidemia AR 11 39
MYH9 Sebastian syndrome, May-Hegglin anomaly, Epstein syndrome, Fechtner syndrome, Macrothrombocytopenia and progressive sensorineural deafness AD 19 113
MYO5A Griscelli syndrome AR 4 4
NBEAL2 Gray platelet syndrome AR 8 38
NBN Breast cancer, Nijmegen breakage syndrome AD/AR 57 62
NF1* Watson syndrome, Neurofibromatosis, Neurofibromatosis-Noonan syndrome AD 261 2607
NHP2 Dyskeratosis congenita AR 3 3
NOP10 Dyskeratosis congenita AR 1 1
NRAS Noonan syndrome AD 17 8
OCA2 Albinism, brown oculocutaneous, Albinism, oculocutaneous, Skin/hair/eye pigmentation AD/AR 24 186
P2RY12 Bleeding disorder, platelet- AD/AR 3 11
PALB2 Fanconi anemia, Pancreatic cancer, Breast cancer AD/AR 237 223
PC Pyruvate carboxylase deficiency AR 24 39
PDHA1 Leigh syndrome, Pyruvate dehydrogenase E1-alpha deficiency XL 39 165
PDHX Pyruvate dehydrogenase E3-binding protein deficiency AR 12 22
PKLR Pyruvate kinase deficiency AR 16 240
PMS2* Mismatch repair cancer syndrome, Colorectal cancer, hereditary nonpolyposis AD/AR 151 266
PRF1 Lymphoma, non-Hodgkin, Aplastic anemia, adult-onset, Hemophagocytic lymphohistiocytosis AR 15 165
PROC Thrombophilia, hereditary AD/AR 29 374
PROS1* Thrombophilia, hereditary AD/AR 15 409
PTPN11 LEOPARD syndrome, Noonan syndrome, Metachondromatosis AD 122 129
PUS1 Mitochondrial myopathy and sideroblastic anemia AR 5 7
RAB27A Griscelli syndrome, Elejalde syndrome AR 10 45
RAD51C Fanconi anemia, Breast-ovarian cancer, familial AD/AR 49 86
RBM8A* Thrombocytopenia - absent radius AD/AR 4 7
RECQL4 Baller-Gerold syndrome, RAPADILINO syndrome, Rothmund-Thomson syndrome AR 34 92
RPL5 Diamond-Blackfan anemia AD 8 66
RPL11 Diamond-Blackfan anemia AD 7 40
RPL15* Diamond-Blackfan anemia AD 2 2
RPL35A Diamond-Blackfan anemia AD 4 12
RPS7 Diamond-Blackfan anemia AD 1 8
RPS10 Diamond-Blackfan anemia AD 3 5
RPS17* Diamond-Blackfan anemia AD 4 17
RPS19 Diamond-Blackfan anemia AD 9 166
RPS24 Diamond-Blackfan anemia AD 5 9
RPS26 Diamond-Blackfan anemia AD 8 30
RPS29 Diamond-Blackfan anemia AD 2 3
RTEL1 Pulmonary fibrosis and/or bone marrow failure, Dyskeratosis congenita AD/AR 27 26
RUNX1 Platelet disorder, familial, with associated myeloid malignancy AD 13 74
SBDS* Aplastic anemia, Shwachman-Diamond syndrome, Severe spondylometaphyseal dysplasia AD/AR 12 88
SEC23B Anemia, dyserythropoietic congenital AR 12 88
SERPINC1 Antithrombin III deficiency AD/AR 39 355
SFTPB Surfactant metabolism dysfunction, pulmonary AR 5 30
SFTPC Surfactant metabolism dysfunction, pulmonary AD 7 81
SH2D1A Lymphoproliferative syndrome XL 14 120
SLC4A1 Spherocytosis, Ovalcytosis, Renal tubular acidosis, distal, with hemolytic anemia, Cryohydrocytosis AD/AR/BG 30 136
SLC19A2 Thiamine-responsive megaloblastic anemia syndrome AR 10 47
SLC45A2 Skin/hair/eye pigmentation, Oculocutaneous albinism AD/AR 12 97
SLFN14 Thrombocytopenia AD/AR 4 5
SLX4 Fanconi anemia AR 8 31
SPTA1 Spherocytosis, Ellipsocytosis, Pyropoikilocytosis AD/AR 21 45
SPTB Spherocytosis, Anemia, neonatal hemolytic, Ellipsocytosis AD/AR 14 66
STX11 Hemophagocytic lymphohistiocytosis, familial AR 5 15
STXBP2 Hemophagocytic lymphohistiocytosis, familial AR 8 60
TBXA2R Bleeding disorder, platelet- AD 11
TCIRG1 Osteopetrosis, severe neonatal or infantile forms (OPTB1) AR 9 127
TERC Aplastic anemia, Pulmonary fibrosis and/or bone marrow failure, telomere-related, Dyskeratosis congenita AD 36 60
TERT Aplastic anemia, Pulmonary fibrosis and/or bone marrow failure, telomere-related, Dyskeratosis congenita AD/AR 39 133
THBD Thrombophilia due to thrombomodulin defect, Hemolytic uremic syndrome, atypical AD 5 27
TINF2 Revesz syndrome, Dyskeratosis congenita AD 20 33
TMPRSS6 Iron-refractory iron deficiency anemia AR 13 76
TP53 Colorectal cancer, Li-Fraumeni syndrome, Ependymoma, intracranial, Choroid plexus papilloma, Breast cancer, familial, Adrenocortical carcinoma, Osteogenic sarcoma, Hepatoblastoma, Non-Hodgkin lymphoma AD 148 391
TPI1 Triosephosphate isomerase deficiency AR 8 19
TUBB1 Macrothrombocytopenia AD 1 9
TYR* Albinism, oculocutaneous AR 46 356
TYRP1 Albinism, oculocutaneous AR 7 28
UNC13D Hemophagocytic lymphohistiocytosis, familial AR 9 139
USB1 Poikiloderma with neutropenia AR 4 21
VKORC1 Drug metabolism, VKORC1-related, Vitamin K-dependent clotting factors, combined deficiency AD/AR 5 33
VWF* Von Willebrand disease AD/AR 38 857
WAS Neutropenia, severe congenital, Thrombocytopenia, Wiskott-Aldrich syndrome XL 32 429
WRAP53 Dyskeratosis congenita AR 5 6
XIAP* Lymphoproliferative syndrome XL 4 78
XRCC2 Hereditary breast cancer AD/AR 3 13
YARS2 Myopathy, lactic acidosis, and sideroblastic anemia AR 19 10

*Some regions of the gene are duplicated in the genome leading to limited sensitivity within the regions. Thus, low-quality variants are filtered out from the duplicated regions and only high-quality variants confirmed by other methods are reported out. Read more.

Gene, refers to HGNC approved gene symbol; Inheritance to inheritance patterns such as autosomal dominant (AD), autosomal recessive (AR) and X-linked (XL); ClinVar, refers to a number of variants in the gene classified as pathogenic or likely pathogenic in ClinVar (; HGMD, refers to a number of variants with possible disease association in the gene listed in Human Gene Mutation Database (HGMD, The list of associated (gene specific) phenotypes are generated from CDG ( or Orphanet ( databases.

Gene Genomic location HG19 HGVS RefSeq RS-number Comment Reference
F2 Chr11:46761055 c.*97G>A NM_000506.4 rs1799963

Blueprint Genetics offers a Comprehensive Hematology Panel that covers classical genes associated with hereditary anemia, inherited bleeding disorder, inherited bone marrow failure syndrome and leukemia. The genes are carefully selected based on the existing scientific evidence, our experience and most current mutation databases. Candidate genes are excluded from this first-line diagnostic test. The test does not recognise balanced translocations or complex inversions, and it may not detect low-level mosaicism. The test should not be used for analysis of sequence repeats or for diagnosis of disorders caused by mutations in the mitochondrial DNA.

Analytical validation is a continuous process at Blueprint Genetics. Our mission is to improve the quality of the sequencing process and each modification is followed by our standardized validation process. Average sensitivity and specificity in Blueprint NGS Panels is 99.3% and 99.9% for detecting SNPs. Sensitivity to for indels vary depending on the size of the alteration: 1-10bps (96.0%), 11-20 bps (88.4%) and 21-30 bps (66.7%). The longest detected indel was 46 bps by sequence analysis. Detection limit for Del/Dup (CNV) analysis varies through the genome depending on exon size, sequencing coverage and sequence content. The sensitivity is 71.5% for single exon deletions and duplications and 99% for three exons’ deletions and duplications. We have validated the assays for different starting materials including EDTA-blood, isolated DNA (no FFPE) and saliva that all provide high-quality results. The diagnostic yield varies substantially depending on the used assay, referring healthcare professional, hospital and country. Blueprint Genetics’ Plus Analysis (Seq+Del/Dup) maximizes the chance to find molecular genetic diagnosis for your patient although Sequence Analysis or Del/Dup Analysis may be cost-effective first line test if your patient’s phenotype is suggestive for a specific mutation profile.

The sequencing data generated in our laboratory is analyzed with our proprietary data analysis and annotation pipeline, integrating state-of-the art algorithms and industry-standard software solutions. Incorporation of rigorous quality control steps throughout the workflow of the pipeline ensures the consistency, validity and accuracy of results. The highest relevance in the reported variants is achieved through elimination of false positive findings based on variability data for thousands of publicly available human reference sequences and validation against our in-house curated mutation database as well as the most current and relevant human mutation databases. Reference databases currently used are the 1000 Genomes Project (, the NHLBI GO Exome Sequencing Project (ESP;, the Exome Aggregation Consortium (ExAC;, ClinVar database of genotype-phenotype associations ( and the Human Gene Mutation Database ( The consequence of variants in coding and splice regions are estimated using the following in silico variant prediction tools: SIFT (, Polyphen (, and Mutation Taster (

Through our online ordering and statement reporting system, Nucleus, the customer can access specific details of the analysis of the patient. This includes coverage and quality specifications and other relevant information on the analysis. This represents our mission to build fully transparent diagnostics where the customer gains easy access to crucial details of the analysis process.

In addition to our cutting-edge patented sequencing technology and proprietary bioinformatics pipeline, we also provide the customers with the best-informed clinical report on the market. Clinical interpretation requires fundamental clinical and genetic understanding. At Blueprint Genetics our geneticists and clinicians, who together evaluate the results from the sequence analysis pipeline in the context of phenotype information provided in the requisition form, prepare the clinical statement. Our goal is to provide clinically meaningful statements that are understandable for all medical professionals, even without training in genetics.

Variants reported in the statement are always classified using the Blueprint Genetics Variant Classification Scheme modified from the ACMG guidelines (Richards et al. 2015), which has been developed by evaluating existing literature, databases and with thousands of clinical cases analyzed in our laboratory. Variant classification forms the corner stone of clinical interpretation and following patient management decisions. Our statement also includes allele frequencies in reference populations and in silico predictions. We also provide PubMed IDs to the articles or submission numbers to public databases that have been used in the interpretation of the detected variants. In our conclusion, we summarize all the existing information and provide our rationale for the classification of the variant.

A final component of the analysis is the Sanger confirmation of the variants classified as likely pathogenic or pathogenic. This does not only bring confidence to the results obtained by our NGS solution but establishes the mutation specific test for family members. Sanger sequencing is also used occasionally with other variants reported in the statement. In the case of variant of uncertain significance (VUS) we do not recommend risk stratification based on the genetic finding. Furthermore, in the case VUS we do not recommend use of genetic information in patient management or genetic counseling. For some cases Blueprint Genetics offers a special free of charge service to investigate the role of identified VUS.

We constantly follow genetic literature adapting new relevant information and findings to our diagnostics. Relevant novel discoveries can be rapidly translated and adopted into our diagnostics without delay. These processes ensure that our diagnostic panels and clinical statements remain the most up-to-date on the market.

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Accepted sample types

  • EDTA blood, min. 1 ml
  • Purified DNA, min. 5μg
  • Saliva (Oragene DNA OG-500 kit)

Label the sample tube with your patient’s name, date of birth and the date of sample collection.

Note that we do not accept DNA samples isolated from formalin-fixed paraffin-embedded (FFPE) tissue.


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