rs11524

A SNP in the LPIN1 gene on chromosome 2. Its most notable genotype is T;T: common in clinvar

Gene
LPIN1
Location
Chr 211,826,191 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
22%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in clinvarTypical · 0.058% of people

On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageT;T 58%
  • European ancestry (Utah)T;T 80%
  • Han Chinese (Beijing)T;T 67%
  • Japanese (Tokyo)T;T 79%
  • Yoruba (Nigeria)T;T 26%
  • African ancestry (Southwest US)T;T 32%
  • Chinese (Denver)T;T 75%
  • Gujarati IndianT;T 86%
  • Luhya (Kenya)T;T 25%
  • Mexican ancestry (Los Angeles)T;T 67%
  • Maasai (Kenya)T;T 27%
  • TuscanT;T 74%

Other LPIN1 SNPs

All LPIN1 SNPs

Notes

From SNPedia

Notes

This SNP is postulated to be responsible for the lower blood pressure seen associated with SNP rs10495584, but direct evidence has not been found.

Source and license

Adapted from rs11524 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.