rs1341665
A SNP on chromosome 1. Its most notable genotype is A;G: common in complete genomics
- Gene
- None listed
- Location
- Chr 1159,721,769 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 38%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;G). 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 40%
- European ancestry (Utah)A;G 49%
- Han Chinese (Beijing)A;G 44%
- Japanese (Tokyo)A;G 30%
- Yoruba (Nigeria)A;G 37%
Source and license
Adapted from rs1341665 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.