rs7776725
A SNP in the FAM3C gene on chromosome 7. Its most notable genotype is C;C: weaker bones
- Gene
- FAM3C
- Location
- Chr 7121,393,067 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 25%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C), (T;T). 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.
- AverageC;C 8% T;T 55%
- European ancestry (Utah)C;C 11% T;T 55%
- Han Chinese (Beijing)C;C <1% T;T 79%
- Japanese (Tokyo)C;C 3% T;T 76%
- Yoruba (Nigeria)C;C 10% T;T 44%
- African ancestry (Southwest US)C;C 19% T;T 35%
- Chinese (Denver)C;C 2% T;T 79%
- Gujarati IndianC;C 3% T;T 62%
- Luhya (Kenya)C;C 12% T;T 43%
- Mexican ancestry (Los Angeles)C;C 12% T;T 52%
- Maasai (Kenya)C;C 12% T;T 37%
- TuscanC;C 8% T;T 49%
Notes
From SNPedia
Notes
Korean bone mineral density rs7776725 and rs1721400
Source and license
Adapted from rs7776725 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.