rs11568492

A SNP in the SLC22A8 gene on chromosome 11. Its most notable genotype is G;G: common in complete genomics

Gene
SLC22A8
Location
Chr 1162,996,085 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in complete genomicsTypical · 0.0100% of people

SNPedia records rs11568492 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 2 HapMap populations.

  • AverageG;G 100%
  • European ancestry (Utah)G;G 100%
  • Han Chinese (Beijing)G;G 100%

Other SLC22A8 SNPs

All SLC22A8 SNPs

Source and license

Adapted from rs11568492 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.