rs267607326
A SNP in the VWF gene on chromosome 12. Its most notable genotype is C;T: von Willebrand disease
- Gene
- VWF
- Location
- Chr 126,022,841 (GRCh38)
- Highest magnitude
- 3.5Important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TGoodcommon in clinvar
- C;TMost notableBadvon Willebrand disease
- C;CBadVon Willebrand disease, type 2A
SNPedia records rs267607326 on the minus strand: (A;A), (A;G), (G;G). 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
- rs61748477A;AVon Willebrand disease, type 2NVery 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
Notes
From SNPedia
Notes
rs267607326, also known as c.3437A>G, p.Tyr1146Cys and Y1146C, is a SNP in the VWF gene on chromosome 12. The rare rs267607326(G) allele is considered pathogenic for Von Willebrand disease, type 2A, according to ClinVar and the VWFdb.
C;C
see discussion at rs267607326
Source and license
Adapted from rs267607326 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.