EQA Scheme Program 2026 PDF
EQA Scheme
Engraftment- and Chimerism Diagnostics (618)
HLA Diagnostics - High resolution, molecular HLA typing class I and II (444)
HLA Diagnostics - HLA-DQ (772)
HLA Diagnostics - Low resolution, molecular HLA typing class I and II (442)
Immunohaematology 03 - Platelet Immunology (233)
Immunohaematology 06 - Molecular Diagnostic (235)
Molecular Genetics - Aldolase B-Gene (ALDOB) (A149P, A174D, N334K) (793)
Molecular Genetics - Alpha-Globin and beta-Globin (794)
Molecular Genetics - Alpha1-Antitrypsin-Gene (SERPINA1) (PiM, PiS, PiZ) (743)
Molecular Genetics - Angiotensin Converting Enzyme (763)
Molecular Genetics - Antithrombin (AT3; SERPINC1 Gene) (792)
Molecular Genetics - Apolipoprotein B APOB, R3500Q (HGVS: c.10580G>A; p.Arg3527Gln), R3500W (HGVS: c.10579C>T; p.Arg3527Trp)) (771)
Molecular Genetics - Apolipoprotein E-Gene (APOE) (E2, E3, E4) (744)
Molecular Genetics - Apolipoprotein E-Gene (APOE) (E2, E3, E4) - whole blood (734)
Molecular Genetics - AZF (Y-Chromosome Microdeletions) (788)
Molecular Genetics - BRCA1 BRCA2 (779)
Molecular Genetics - C-C Motif Chemokine Receptor 5 (764)
Molecular Genetics - CFTR Common Mutations (778)
Molecular Genetics - Collagen Receptor-Gene (ITGA2) C807T (739)
Molecular Genetics - Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency (CYP21A2 Gene) (773)
Molecular Genetics - Connexin 26 (GJB2 Gene, GJB6 Gene) (782)
Molecular Genetics - Copper-Binding Protein: ATP7B-Gene (ATP7) (H1069Q) (745)
Molecular Genetics - ctDNA Tumour Panel (752)
Molecular Genetics - CYP2C9 CYP2C19 VKORC1 TPMT (775)
Molecular Genetics - CYP2D6 IL28B (777)
Molecular Genetics - Determination of Fetal Sex (728)
Molecular Genetics - Dihydropyrimidin Dehydrogenase (762)
Molecular Genetics - Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) (DMD Gene) (780)
Molecular Genetics - Factor V-Leiden-Gene (F5) (740)
Molecular Genetics - Factor V-Leiden-Gene (F5) - Whole Blood (730)
Molecular Genetics - Fibrinogen Receptor-Gene (ITGB3) HPA 1a/1b (749)
Molecular Genetics - Fragile X Syndrome (FMR1 Gene, CGG Repeats) (781)
Molecular Genetics - Hereditary Fever Syndroms (706)
Molecular Genetics - HFE-Gene: H63D, C282Y (741)
Molecular Genetics - HFE-Gene: H63D, C282Y (optional: S65C) - whole blood (733)
Molecular Genetics - Huntington Disease (HTT Gene, CAG Repeats) (784)
Molecular Genetics - Lactase-Gene -13910T>C (MCM6 Gene, IVS13 C-T, rs4988235, HGVS: C.1917+326 C>T) (770)
Molecular Genetics - MLH1 MSH2 MSH6 PMS2 (Lynch) (783)
Molecular Genetics - MTHFR-Gene C677T (optional A1298C) (747)
Molecular Genetics - MTHFR-Gene C677T (optional A1298C) - whole blood (732)
Molecular Genetics - NIPT - Determination of Fetal RhD Status (727)
Molecular Genetics - NOD2 (774)
Molecular Genetics - PAI-1-Gene (SERPINE1) (4G/5G) (748)
Molecular Genetics - PAI-1-Gene (SERPINE1) (4G/5G) - whole blood (735)
Molecular Genetics - Prader-Willi (PWS) und Angelman (AS) Syndromes (Chromosome region 15q11-13, SNRPN) (786)
Molecular Genetics - Protein C (PROC Gene) (790)
Molecular Genetics - Protein S (PROS1 Gene) (791)
Molecular Genetics - Prothrombin-Gene (F2) G20210A (746)
Molecular Genetics - Prothrombin-Gene (F2) G20210A - whole blood (731)
Molecular Genetics - Ret Proto-Oncogene (Multiple Endocrine Neoplasia Type 2, MEN2, RET Gene) (738)
Molecular Genetics - Spinal Muscular Atrophy (SMN1 and SMN2 Genes) (787)
Molecular Genetics - UDP-Glucuronyltransferase 1-Gene (UGT1A1) (742)
Molecular Genetics - UDP-Glucuronyltransferase 1-Gene (UGT1A1) – Whole Blood (726)
Molecular Genetics – FLT3 (internal tandem duplication) (701)
Molecular Oncology - AML-Panel (NGS) (798)
Molecular Oncology - BRAF (795)
Molecular Oncology - BTK (796)
Molecular Oncology - KIT (767)
Molecular Oncology - MYD88 (766)
Molecular Oncology - Myeloproliferative Neoplasia (768)
Molecular Oncology - SF3B1 (797)
Molecular Oncology - STAT3 (769)
Molecular Oncology - TP53 (765)
