rs61748477
A SNP in the VWF gene on chromosome 12. Its most notable genotype is A;A: Von Willebrand disease, type 2N
- Gene
- VWF
- Location
- Chr 126,044,361 (GRCh38)
- Highest magnitude
- 4.0Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- A;GBadcarrier of a Von Willebrand disease allele
- A;AMost notableBadVon Willebrand disease, type 2N
SNPedia records rs61748477 on the minus strand: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other VWF SNPs
- rs41276738T;TVon Willebrand disease, type 1Very important
- rs61748478C;CVon Willebrand disease, type 2NVery important
- rs61748497G;GVon Willebrand disease, type 2NVery important
- rs61750584G;GVon Willebrand disease, type 2AVery important
- rs61750595A;Alikely miscall in Ancestry V2.0 datasets; otherwise, Von Willebrand disease, type 3Very important
- rs61750612A;AVon Willebrand disease, type 3Very important
- rs61750630A;AVon Willebrand disease, type 3Very important
- rs61751296A;AVon Willebrand disease, type 3Very important
Notes
From SNPedia
Notes
rs61748477, also known as c.2372C>T, Thr791Met and T791M, is a SNP in the VWF gene on chromosome 12. The rare rs61748477(T) allele is considered pathogenic for Von Willebrand disease, type 2N, according to ClinVar and the VWFdb. This SNP is also referred to as i5049057 by 23andMe.
A;G
see discussion at rs61748477
A;A
see discussion at rs61748477
Source and license
Adapted from rs61748477 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.