EQA Scheme Program

EQAS/PT Program 2027

Pricelist 2027 for Participants

Shipping Costs 2027

 

EQA Scheme

Engraftment- and Chimerism Diagnostics (618)

Engraftment Diagnostics Chimerism Diagnostics Dr. med. Roland Reibke Dr. rer. biol. hum. Andrea Dick

EQA Scheme

Immunohaematology 06 - Molecular Diagnostic (235)

Immunohaematology 06 - Molecular Diagnostic HPA - system HNA - system Granulocyte - alleles Erythocyte - alleles A B 0 - system MNS - system RHCE RHD RHD - Deletion Thrombocyte - alleles MNS system [GYP] Kell system [KEL] Duffy system [FY] Kidd system [JK] Lutheran system [Lu] Diego system [DI] Yt system [YT] Dombrock system [DO] Colton system [CO] Landsteiner Wiener system [LW] Knops system [KN] Vel system [VEL] rare erythrocyte blood group systems Prof. Dr. med. Ulrich Sachs Prof. Dr. med. Willy A. Flegel

EQA Scheme

Molecular Genetics - Aldolase B (ALDOB) Variants (A149P, A174D, N334K) (793)

Aldolase B A149P A174D N334K Aldolase B (A149P, A174D, N334K) ALDOB Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Alpha-Globin and beta-Globin (794)

beta-Globin alpha-Globin HBA HBB Dr. med. Claudia Frömmel Dr. Adriana Méndez

EQA Scheme

Molecular Genetics - Alpha1-Antitrypsin (SERPINA1) Variants (PiM, PiS, PiZ) (743)

alpha1-Antitrypsin a1-AT Z-Locus a1-AT S-Locus AAT a1PI alpha1-proteinase-Inhibitor Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Angiotensin Converting Enzyme (763)

ACE INS/DEL Angiotensin Converting Enzym Apolipoprotein Prof. Dr. med. Folker Wenzel

EQA Scheme

Molecular Genetics - Antithrombin (AT3; SERPINC1 Gene) (792)

AT3 Antithrombin SERPINC1 thrombosis thrombophilia clotting factor hemostasis SERPINC1 gene Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Apolipoprotein (APOE) Variants (E2, E3, E4) - Whole Blood (734)

Apolipoprotein E Apolipoprotein E ApoE (genotype 2, 3, 4) Apo-E Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Apolipoprotein B APOB, R3500Q (HGVS: c.10580G>A; p.Arg3527Gln), R3500W (HGVS: c.10579C>T; p.Arg3527Trp)) (771)

Apo B ApoB APOB hypercholesterolemia Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Apolipoprotein E (APOE) Variants (E2, E3, E4) (744)

Apo E (Genotyp 2, 3, 4) ApoE (genotype 2, 3, 4) Apolipoprotein E Apolipoprotein E Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - AZF (Y-Chromosome Microdeletions) (788)

AZF Azoospermia factor autoprothrombin IIA blood coagulation factor XIV PD Dr. rer. nat. Julia Hentschel MSc. Simone Ahting

EQA Scheme

Molecular Genetics - BRCA1 BRCA2 (779)

BRCA2 BRCA1 HBOC breast and ovarian cancer Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - C-C Motif Chemokine Receptor 5 (764)

CCR5-Gene chemokine receptor Prof. Dr. med. Folker Wenzel

EQA Scheme

Molecular Genetics - CFTR Common Mutations (778)

CFTR gene CFTR Common Mutations Cystic fibrosis PD Dr. rer. nat. Julia Hentschel MSc. Simone Ahting

EQA Scheme

Molecular Genetics - Collagen Receptor (ITGA2) Variant C807T (739)

Collagen receptor GP Ia/IIa (C 807 T) Collagen Receptor C807T GP Ia/IIa Collagen receptor C807T Collagen receptor GP Ia/IIa Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency (CYP21A2 Gene) (773)

Cyp21A2 CAH congenital adrenal hyperplasia 21-hydroxylase deficiency CYP21A2 gene Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Connexin 26 (GJB2 Gene, GJB6 Gene) (782)

Connexin 26 non-syndromic hearing inpairment GJB2 GJB6 DFNB1 GJB2 gene GJB6 gene Gap junction beta-2 protein GJB2 Cx26 Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Copper-Binding Protein ATP7B Variant (H1069Q) (745)

ATP 7 B: H 1069 Q Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics - ctDNA Tumour Panel (752)

Liquid Biopsy ctDNA (liquid biopsy) Tumor Panel (liquid biopsy) PIK3CA (liquid biopsy) KRAS Codon 13 (liquid biopsy) ESR1 (liquid biopsy) KRAS Codon 61 (liquid biopsy) EGFR T790M (liquid biopsy) BRAF V600 (liquid biopsy) KRAS Codon 12 (liquid biopsy) Prof. Dr. med. Stefan Holdenrieder

EQA Scheme

Molecular Genetics - CYP2C9 CYP2C19 VKORC1 TPMT (775)

CYP2C9 CYP2C19 VKORC1 TPMT Pharmacogenetics Prof. Dr. med. Folker Wenzel

EQA Scheme

Molecular Genetics - CYP2D6 IL28B (777)

CYP2D6 IL28B DPD Prof. Dr. med. Folker Wenzel

EQA Scheme

Molecular Genetics - Dihydropyrimidin Dehydrogenase (762)

Dihydropyrimidin Dehydrogenase DPYD Dr. rer. nat. Susanna Schubert PD Dr. rer. nat. Julia Hentschel

EQA Scheme

Molecular Genetics - Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) (DMD Gene) (780)

Dystrophin DMD Duchenne muscular dystrophy (DMD) Becker muscular dystrophy (BMD) muscular dystrophy Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Factor V-Leiden (F5) Variant (740)

Factor V-Leiden Factor V-Leiden thrombophilia thrombosis Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Factor V-Leiden (F5) Variant - Whole Blood (730)

Factor V-Leiden thrombophilia thrombosis Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Fibrinogen Receptor (ITGB3) Variant HPA 1a/1b (749)

HPA Fibrinogen Receptor HPA 1a/1b Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Fragile X Syndrome (FMR1 Gene, CGG Repeats) (781)

Fragile X FMR1 FXS FXTAS FXPOI CGG-Repeat Fragile X syndrom Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics - Hereditary Fever Syndroms (706)

Prof. Dr. med. Folker Wenzel Dr. rer. nat. Morten O. Christensen

EQA Scheme

Molecular Genetics - HFE Variants H63D, C282Y (optional: S65C) (741)

HFE H63D C282Y S65C HFE (C282Y, H63D, S65C) hereditary hemochromatosis Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - HFE Variants H63D, C282Y (optional: S65C) - Whole Blood (733)

HFE: S 65 C HFE: H 63 D HFE: C 282 Y C282Y HFE (C282Y, H63D, S65C) hereditary hemochromatosis Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Huntington Disease (HTT Gene, CAG Repeats) (784)

HTT Huntingtin HTT Huntington disease (HD) Expansion of trinucleotide CAG repeats Huntingtin HTT gene IT15 HD Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Lactase-Variant -13910T>C (MCM6 Gene, IVS13 C-T, rs4988235, HGVS: C.1917+326 C>T) (770)

Lactase-gene LCT Lactose intollerance Lactose Lactase gene lactose intolerance Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - MLH1 MSH2 MSH6 PMS2 (Lynch) (783)

MLH1 MSH2 PMS2 HNPCC MSH6 Hereditary nonpolyposis colorectal cancer Lynch syndrome PD Dr. rer. nat. Julia Hentschel MSc. Simone Ahting

EQA Scheme

Molecular Genetics - MTHFR Variants C677T (optional A1298C) (747)

A1298C MTHFR C677T MTHFR (C677T, A1298C) Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - MTHFR Variants C677T (optional A1298C) - Whole Blood (732)

A1298C MTHFR MTHFR C677T MTHFR (C677T, A1298C) Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - NIPT - Determination of Fetal RhD Status (727)

Prof. Dr. med. Folker Wenzel Prof. Dr. rer. nat. Ingo Schellenberg

EQA Scheme

Molecular Genetics - NOD2 (774)

Prof. Dr. med. Folker Wenzel

EQA Scheme

Molecular Genetics - PAI-1 (SERPINE1) Variant (4G/5G) (748)

PAI-1 (4G/5G) Plasminogenactivator-Inhibitor (PAI): 4G, 5G Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - PAI-1 (SERPINE1) Variant (4G/5G) - Whole Blood (735)

PAI-1 (4G/5G) Plasminogenactivator-Inhibitor (PAI): 4G, 5G PAI-1 (4G/5G) Plasminogenactivator inhibitor (PAI): 4G, 5G Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Prader-Willi (PWS) und Angelman (AS) Syndromes (Chromosome region 15q11-13, SNRPN) (786)

SNRPN Prader-Willi syndrome (PWS) Angelmann syndrome (AS) ANCR Prader–Labhart–Willi-Fanconi syndrome Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Protein C (PROC Gene) (790)

clotting factor Protein C PROC coagulation thrombosis thrombophilia hemostasis PROC gene Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Protein S (PROS1 Gene) (791)

Protein S PROC coagulation thrombosis thrombophilia clotting factor hemostasis PROS1 gene PROS Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Prothrombin (F2) Variant G20210A (746)

Prothrombin G20210A thrombophilia thrombosis Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Prothrombin (F2) Variant G20210A - Whole Blood (731)

Prothrombin G20210A Prothrombin G20210A thrombophilia thrombosis Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Ret Proto-Oncogene (Multiple Endocrine Neoplasia Type 2, MEN2, RET Gene) (738)

MEN2A Multiple Endocrine Neoplasia Type 2A Ret Proto-Oncogene RET MEN2 Syndrome Sipple syndrome Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - Spinal Muscular Atrophy (SMN1 and SMN2 Genes) (787)

SMN1 SMN2 spinal muscular atropy SMA SMN SMN1 and SMN2 genes Survival of motor neuron Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Genetics - UDP-Glucuronyltransferase 1 (UGT1A1) Variants (742)

UDP-Glucuronyltransferase 1 UDP-glucuronyltransferase 1 (*28, *6) UDPG1 (*28, *6) UDP-GT1 Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics - UDP-Glucuronyltransferase 1 (UGT1A1) variants – Whole Blood (726)

UDP-glucuronyltransferase 1 (*28, *6) UDPG1 (*28, *6) Dr. rer. nat. Ralf Flörke Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics – Factor IX-Gene (F9) (673)

F9 Factor IX coagulation clotting factor bleeding tendency hemostasis Hemophilia B Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics – Factor V-Gene (F5) (670)

F5 Factor V coagulation clotting factor bleeding tendency hemostasis Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics – Factor VII-Gene (F7) (671)

F7 Factor VII coagulation clotting factor bleeding tendency hemostasis Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics – Factor VIII-Gene (F8) (672)

F8 Factor VIII coagulation clotting factor bleeding tendency hemostasis Hemophilia A Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics – Factor X-Gene (F10) (674)

F10 Factor X coagulation clotting factor bleeding tendency hemostasis Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics – Factor XI-Gene (F11) (675)

F11 Factor XI coagulation clotting factor bleeding tendency hemostasis Hemophilia C Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics – Factor XIII-Gene (F13A1, F13B) (677)

F13A1 F13B Factor XIII coagulation clotting factor bleeding tendency hemostasis Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics – Fibrinogen-Gene (FGA, FGB, FGG) (676)

FGA FGB FGG Fibrinogen coagulation clotting factor bleeding tendency hemostasis Hypofibrinogenemia Dysfibrinogenemia Hypodysfibrinogenemia Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

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Molecular Genetics – FLT3 (internal tandem duplication) (701)

FLT3-ITD FLT3 (internal tandem duplication) Prof. Dr. Karl-Anton Kreuzer Dr. rer. nat. Eva Lorsy

EQA Scheme

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Molecular Genetics – NIPT - Aneuploidies, fetal sex and fetal fraction (728)

Prof. Dr. med. Folker Wenzel Prof. Dr. rer. nat. Ingo Schellenberg

EQA Scheme

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Molecular Genetics – von Willebrand Factor-Gene (VWF) (678)

VWF von Willebrand factor von Willebrand syndrome vWS coagulation clotting factor bleeding tendency hemostasis Dr. rer. nat. Morten O. Christensen Dr. med. Günther Kappert

EQA Scheme

Molecular Oncology - AML-Panel (NGS) (798)

CEBPA (CDS) Mutation(s) FLT3 (TKD) Mutation(s) IDH1 Exon 4 Mutation(s) IDH2 Exon 4 Mutation(s) NPM1 Exon 11 Mutation(s) RUNX1 (CDS) Mutation(s) TP53 (CDS) Mutation(s) ASXL1 Nomenclature CEBPA Nomenclature FLT3 Nomenclature IDH1 Nomenclature IDH2 Nomenclature NPM1 Nomenclature RUNX1 Nomenclature TP53 Nomenclature AML-Panel (NGS) Acute myeloid leukemia Next Generation Sequencing Prof. Dr. Karl-Anton Kreuzer Dr. rer. nat. Eva Lorsy

EQA Scheme

Molecular Oncology - BRAF (795)

BRAF BRAF Nomenclature BRAF p.V600 BRAF p.V600 Prof. Dr. Karl-Anton Kreuzer Dr. rer. nat. Eva Lorsy

EQA Scheme

Molecular Oncology - BTK (796)

BTK BTK Nomenclature BTK p.C481 Bruton tyrosine kinase Prof. Dr. Karl-Anton Kreuzer Dr. rer. nat. Eva Lorsy

EQA Scheme

Molecular Oncology - KIT (767)

KIT p.D816V tyrosine kinase Prof. Dr. Karl-Anton Kreuzer Dr. rer. nat. Eva Lorsy

EQA Scheme

Molecular Oncology - MYD88 (766)

MYD88 p.L265P Prof. Dr. Karl-Anton Kreuzer Dr. rer. nat. Eva Lorsy

EQA Scheme

Molecular Oncology - Myeloproliferative Neoplasia (768)

CALR JAK2 MPL MPN Myeloproliferative Neoplasia Prof. Dr. Karl-Anton Kreuzer Dr. rer. nat. Eva Lorsy

EQA Scheme

Molecular Oncology - SF3B1 (797)

SF3B1 SF3B1 Exon 14-15 SF3B1 Nomenclature Prof. Dr. Karl-Anton Kreuzer Dr. rer. nat. Eva Lorsy

EQA Scheme

Molecular Oncology - STAT3 (769)

STAT3 transcription factor Prof. Dr. Karl-Anton Kreuzer Dr. rer. nat. Eva Lorsy

EQA Scheme

Molecular Oncology - TP53 (765)

TP53 tumor suppressor Prof. Dr. Karl-Anton Kreuzer Dr. rer. nat. Eva Lorsy

EQA Scheme

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Molecular Oncology – PML::RARA qualitative (702)

PML::RARA gene fusion PML::RARA qualitative Prof. Dr. Karl-Anton Kreuzer Dr. rer. nat. Eva Lorsy

EQA Scheme

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Molecular Pathology – PIK3CA and ESR1 (590)

Dr. Harald Bartsch