rs11063112
A SNP in the FGF23 gene on chromosome 12. Its most notable genotype is T;T: common in clinvar
- Gene
- FGF23
- Location
- Chr 124,368,914 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
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 11 HapMap populations.
- AverageT;T 70%
- European ancestry (Utah)T;T 56%
- Han Chinese (Beijing)T;T 65%
- Japanese (Tokyo)T;T 80%
- Yoruba (Nigeria)T;T 79%
- African ancestry (Southwest US)T;T 79%
- Chinese (Denver)T;T 67%
- Gujarati IndianT;T 58%
- Luhya (Kenya)T;T 76%
- Mexican ancestry (Los Angeles)T;T 66%
- Maasai (Kenya)T;T 85%
- TuscanT;T 56%
Related
Other FGF23 SNPs
- rs28937882A;GAutosomal dominant hypophosphatemic rickets (predicted)Very important
- rs104894347C;TAutosomal dominant hypophosphatemic rickets (predicted)Very important
- rs193922701C;GAutosomal dominant hypophosphatemic rickets (predicted)Very important
- rs193922702C;TAutosomal dominant hypophosphatemic rickets (predicted)Very important
- rs104894342C;TCarrier of a tumoral calcinosis mutationImportant
- rs104894343A;GCarrier of a tumoral calcinosis mutationImportant
- rs104894344A;GCarrier of a tumoral calcinosis mutationImportant
- rs863224872C;TCarrier of a tumoral calcinosis mutationImportant
Source and license
Adapted from rs11063112 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.