rs11568377
A SNP in the ABCB11 gene on chromosome 2. Its most notable genotype is G;G: common in clinvar
- Gene
- ABCB11
- Location
- Chr 2168,996,710 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs11568377 on the minus strand: (C;C). 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.
- AverageG;G 84%
- Han Chinese (Beijing)G;G 99%
- Yoruba (Nigeria)G;G 67%
- African ancestry (Southwest US)G;G 70%
- Chinese (Denver)G;G 99%
- Gujarati IndianG;G 96%
- Luhya (Kenya)G;G 59%
- Mexican ancestry (Los Angeles)G;G 98%
- Maasai (Kenya)G;G 81%
Related
Other ABCB11 SNPs
- rs497692T;Tcommon in clinvarTypical
- rs2287616A;Acommon in clinvarTypical
- rs2287622G;G2.8x higher risk for intrahepatic cholestasis of pregnancyTypical
- rs3815676T;TNo summary available.Typical
- rs11568372T;Tcommon in clinvarTypical
- rs16856247C;Ccommon in complete genomicsTypical
- rs16856332T;TNo summary available.Typical
Source and license
Adapted from rs11568377 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.