rs1041163
A SNP in the VCAM1 gene on chromosome 1. Its most notable genotype is T;T: common in complete genomics
- Gene
- VCAM1
- Location
- Chr 1100,718,269 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 19%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageT;T 76%
- European ancestry (Utah)T;T 86%
- Han Chinese (Beijing)T;T 82%
- Japanese (Tokyo)T;T 68%
- Yoruba (Nigeria)T;T 68%
Related
Notes
From SNPedia
Show notes, about 170 words
Gene-environment interaction effects on the development of immune responses in the 1st year of life. Prognostic significance of host immune gene polymorphisms in follicular lymphoma survival. Host immune gene polymorphisms in combination with clinical and demographic factors predict late survival in diffuse large B-cell lymphoma patients in the pre-rituximab era. Variants in inflammation genes and the risk of biliary tract cancers and stones: a population-based study in China. Organochlorine exposure, immune gene variation, and risk of non-Hodgkin lymphoma. A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients. Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study. A candidate gene association study of 77 polymorphisms in migraine. Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
Source and license
Adapted from rs1041163 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.