rs9919713

A SNP in the SCARB1 gene on chromosome 12. Its most notable genotype is A;A: common in complete genomics

Gene
SCARB1
Location
Chr 12124,788,217 (GRCh38)
Highest magnitude
0.0Typical
Tested on
Not on consumer chips
Minor allele frequency
25%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in complete genomicsTypical · 0.045% of people

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

Frequency

Share of each genotype in 4 HapMap populations.

  • AverageA;A 45%
  • European ancestry (Utah)A;A 91%
  • Han Chinese (Beijing)A;A 36%
  • Japanese (Tokyo)A;A 23%
  • Yoruba (Nigeria)A;A 31%

Conditions, medicines and genes

Other SCARB1 SNPs

All SCARB1 SNPs

Notes

From SNPedia

Notes

Associations were found between rs9919713 and fasting glucose (P = 2.3 x 10–4) and type-2 diabetes (P = 9.0 x 10–3) in Mexican-American women. In Mexican-American men from the Rancho Bernardo population, the opposite effect was found. Impact of gene variants on sex-specific regulation of human Scavenger receptor class B type 1 (SR-BI) expression in liver and association with lipid levels in a population-based study.

Source and license

Adapted from rs9919713 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.