rs1005651

A SNP in the PRKCA gene on chromosome 17. Its most notable genotype is A;A: common in complete genomics

Gene
PRKCA
Location
Chr 1766,441,893 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
29%

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 11 HapMap populations.

  • AverageA;A 45%
  • European ancestry (Utah)A;A 41%
  • Han Chinese (Beijing)A;A 51%
  • Japanese (Tokyo)A;A 54%
  • Yoruba (Nigeria)A;A 46%
  • African ancestry (Southwest US)A;A 56%
  • Chinese (Denver)A;A 55%
  • Gujarati IndianA;A 16%
  • Luhya (Kenya)A;A 33%
  • Mexican ancestry (Los Angeles)A;A 59%
  • Maasai (Kenya)A;A 35%
  • TuscanA;A 55%

Other PRKCA SNPs

All PRKCA SNPs

Source and license

Adapted from rs1005651 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.