rs11045819
A SNP in the SLCO1B1 gene on chromosome 12. Its most notable genotype is C;C: common on affy axiom data
- Gene
- SLCO1B1
- Location
- Chr 1221,176,879 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 8%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 10 HapMap populations.
- AverageC;C 88%
- European ancestry (Utah)C;C 66%
- Han Chinese (Beijing)C;C 98%
- Japanese (Tokyo)C;C 100%
- Yoruba (Nigeria)C;C 87%
- African ancestry (Southwest US)C;C 84%
- Gujarati IndianC;C 90%
- Luhya (Kenya)C;C 96%
- Mexican ancestry (Los Angeles)C;C 88%
- Maasai (Kenya)C;C 96%
- TuscanC;C 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
- rs11045818G;Gcommon in clinvarTypical
Source and license
Adapted from rs11045819 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.