rs1063857
A SNP in the VWF gene on chromosome 12. Its most notable genotype is A;A: common in clinvar
- Gene
- VWF
- Location
- Chr 126,044,348 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 34%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs1063857 on the minus strand: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageA;A 49%
- European ancestry (Utah)A;A 43%
- Han Chinese (Beijing)A;A 89%
- Japanese (Tokyo)A;A 85%
- Yoruba (Nigeria)A;A 14%
- African ancestry (Southwest US)A;A 14%
- Chinese (Denver)A;A 85%
- Gujarati IndianA;A 67%
- Luhya (Kenya)A;A 15%
- Mexican ancestry (Los Angeles)A;A 60%
- Maasai (Kenya)A;A 30%
- TuscanA;A 42%
Related
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
Source and license
Adapted from rs1063857 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.