rs3802230

A SNP in the CYP11B2 gene on chromosome 8. Its most notable genotype is C;C: common in clinvar

Gene
CYP11B2
Location
Chr 8142,911,448 (GRCh38)
Highest magnitude
0.0Typical
Tested on
AncestryDNA
Minor allele frequency
43%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.018% of people

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 11 HapMap populations.

  • AverageC;C 18%
  • European ancestry (Utah)C;C 20%
  • Han Chinese (Beijing)C;C 39%
  • Japanese (Tokyo)C;C 37%
  • Yoruba (Nigeria)C;C 0%
  • African ancestry (Southwest US)C;C 5%
  • Chinese (Denver)C;C 24%
  • Gujarati IndianC;C 19%
  • Luhya (Kenya)C;C 3%
  • Mexican ancestry (Los Angeles)C;C 24%
  • Maasai (Kenya)C;C 9%
  • TuscanC;C 14%

Other CYP11B2 SNPs

All CYP11B2 SNPs

Source and license

Adapted from rs3802230 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.