rs7646054
A SNP in the ARHGEF3 gene on chromosome 3. Its most notable genotype is A;A: normal
- Gene
- ARHGEF3
- Location
- Chr 356,775,600 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 31%
Genotypes
As shown in 23andMe and AncestryDNA files.
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 13% A;G 37% G;G 50%
- European ancestry (Utah)A;A 27% A;G 38% G;G 35%
- Han Chinese (Beijing)A;A 5% A;G 29% G;G 67%
- Japanese (Tokyo)A;A 3% A;G 19% G;G 79%
- Yoruba (Nigeria)A;A 4% A;G 36% G;G 60%
- African ancestry (Southwest US)A;A 11% A;G 51% G;G 39%
- Chinese (Denver)A;A 5% A;G 38% G;G 57%
- Gujarati IndianA;A 21% A;G 42% G;G 37%
- Luhya (Kenya)A;A 8% A;G 39% G;G 53%
- Mexican ancestry (Los Angeles)A;A 29% A;G 36% G;G 35%
- Maasai (Kenya)A;A 15% A;G 44% G;G 41%
- TuscanA;A 12% A;G 40% G;G 48%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs7646054 is a SNP in the ARHGEF3 gene. A study of 769 Australian female siblings found that the rs7646054(G) allele was significantly associated with lower bone mineral density (BMD) and thus osteoporosis in an age-related manner. Significant associations with hip and spine BMD were confirmed (p = 0.003-0.038), as well as an association with fracture rate (p = 0.02).
Source and license
Adapted from rs7646054 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.