rs9594782
A SNP in the TNFSF11 gene on chromosome 13. Its most notable genotype is T;T.
- Gene
- TNFSF11
- Location
- Chr 1342,577,050 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 5%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 3 HapMap populations.
- AverageT;T 89%
- Han Chinese (Beijing)T;T 87%
- Japanese (Tokyo)T;T 81%
- Yoruba (Nigeria)T;T 98%
Related
Notes
From SNPedia
Notes
Variation in genes involved in the RANKL/RANK/OPG bone remodeling pathway are associated with bone mineral density at different skeletal sites in men. Robust and comprehensive analysis of 20 osteoporosis candidate genes by very high-density single-nucleotide polymorphism screen among 405 white nuclear families identified significant association and gene-gene interaction. Quantitative trait loci, genes, and polymorphisms that regulate bone mineral density in mouse.
Source and license
Adapted from rs9594782 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.