rs7105934
A SNP in the LOC102724265 gene on chromosome 11. Its most notable genotype is A;A: 0.48 times lower odds of developing renal cell carcinoma
- Gene
- LOC102724265
- Location
- Chr 1169,424,973 (GRCh38)
- Highest magnitude
- 2.1Worth knowing
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 21%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableGood0.48 times lower odds of developing renal cell carcinoma
- A;GGood0.69 times lower odds of developing renal cell carcinoma
- G;GGoodcommon in complete genomics
On SNPedia: (A;A), (A;G), (G;G). 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 16% A;G 22% G;G 62%
- European ancestry (Utah)A;A <1% A;G 10% G;G 89%
- Han Chinese (Beijing)A;A 0% A;G 10% G;G 91%
- Japanese (Tokyo)A;A 0% A;G 4% G;G 97%
- Yoruba (Nigeria)A;A 52% A;G 37% G;G 10%
- African ancestry (Southwest US)A;A 40% A;G 47% G;G 12%
- Chinese (Denver)A;A 0% A;G 14% G;G 86%
- Gujarati IndianA;A 0% A;G 6% G;G 94%
- Luhya (Kenya)A;A 58% A;G 38% G;G 4%
- Mexican ancestry (Los Angeles)A;A 2% A;G 7% G;G 91%
- Maasai (Kenya)A;A 24% A;G 49% G;G 26%
- TuscanA;A 1% A;G 21% G;G 78%
Notes
From SNPedia
Notes
23andMe reports that each A allele at rs7105934 is associated with 0.69 times lower odds of developing renal cell carcinoma (a form of kidney cancer).
Source and license
Adapted from rs7105934 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.