rs11045818
A SNP in the SLCO1B1 gene on chromosome 12. Its most notable genotype is G;G: common in clinvar
- Gene
- SLCO1B1
- Location
- Chr 1221,176,827 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageG;G 89%
- European ancestry (Utah)G;G 65%
- Han Chinese (Beijing)G;G 99%
- Japanese (Tokyo)G;G 100%
- Yoruba (Nigeria)G;G 99%
- African ancestry (Southwest US)G;G 88%
- Gujarati IndianG;G 93%
- Mexican ancestry (Los Angeles)G;G 90%
- Maasai (Kenya)G;G 96%
- TuscanG;G 72%
Related
Other SLCO1B1 SNPs
- rs4363657C;C17x increased myopathy risk for statin usersVery important
- rs4149056C;C17x myopathy risk for statin usersImportant
- rs2291075C;Ccommon in clinvarTypical
- rs2306283A;Acommon in clinvarTypical
- rs4149013A;Acommon in complete genomicsTypical
- rs4149018T;Tcommon genotypeTypical
- rs7489119C;Ccommon genotypeTypical
- rs11045819C;Ccommon on affy axiom dataTypical
Source and license
Adapted from rs11045818 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.