rs3809865
A SNP in the ITGB3 gene on chromosome 17. Its most notable genotype is T;T: common in clinvar
- Gene
- ITGB3
- Location
- Chr 1747,311,220 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 28%
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 9%
- European ancestry (Utah)T;T 8%
- Han Chinese (Beijing)T;T 2%
- Japanese (Tokyo)T;T 7%
- Yoruba (Nigeria)T;T 19%
Related
Notes
From SNPedia
Notes
Multifactor dimensionality reduction-phenomics: a novel method to capture genetic heterogeneity with use of phenotypic variables. Association and gene-gene interaction of SLC6A4 and ITGB3 in autism. High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.
Source and license
Adapted from rs3809865 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.