rs11574129
A SNP in the VDR gene on chromosome 12. Its most notable genotype is A;A: common in clinvar
- Gene
- VDR
- Location
- Chr 1247,843,520 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs11574129 on the minus strand: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 8 HapMap populations.
- AverageA;A 87%
- European ancestry (Utah)A;A 98%
- Han Chinese (Beijing)A;A 72%
- Japanese (Tokyo)A;A 75%
- Yoruba (Nigeria)A;A 100%
- Chinese (Denver)A;A 63%
- Gujarati IndianA;A 98%
- Mexican ancestry (Los Angeles)A;A 95%
- TuscanA;A 98%
Related
Other VDR SNPs
- rs2107301A;A2.5x higher risk for prostate cancerImportant
- rs1544410T;TIncreased risk of low bone mineral density disordersWorth knowing
- rs731236A;GNo summary available.Typical
- rs739837G;Gcommon in clinvarTypical
- rs2228570A;Acommon in clinvarTypical
- rs3847987C;Ccommon in clinvarTypical
- rs4516035C;Cif less milk in teenage females, less bone?Typical
- rs11574085T;Tcommon in complete genomicsTypical
Source and license
Adapted from rs11574129 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.