rs2002675
A SNP on chromosome 3. Its most notable genotype is A;G: common in complete genomics
- Gene
- None listed
- Location
- Chr 3185,911,780 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 29%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2002675 on the minus strand: (C;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.
- AverageA;G 38%
- European ancestry (Utah)A;G 55%
- Han Chinese (Beijing)A;G 24%
- Japanese (Tokyo)A;G 27%
- Yoruba (Nigeria)A;G 45%
Source and license
Adapted from rs2002675 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.