rs1671152

A SNP in the GP6 gene on chromosome 19. Its most notable genotype is G;G: common in complete genomics

Gene
GP6
Location
Chr 1955,014,977 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
14%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in complete genomicsTypical · 0.069% of people
  2. T;TGoodcommon in clinvarTypical · 0.05% of people

On SNPedia: (G;G), (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.

  • AverageG;G 69% T;T 5%
  • European ancestry (Utah)G;G 68% T;T 5%
  • Han Chinese (Beijing)G;G 97% T;T 0%
  • Japanese (Tokyo)G;G 97% T;T 0%
  • Yoruba (Nigeria)G;G 45% T;T 10%
  • African ancestry (Southwest US)G;G 48% T;T 9%
  • Chinese (Denver)G;G 97% T;T 0%
  • Gujarati IndianG;G 52% T;T 7%
  • Luhya (Kenya)G;G 48% T;T 13%
  • Mexican ancestry (Los Angeles)G;G 90% T;T 2%
  • Maasai (Kenya)G;G 47% T;T 10%
  • TuscanG;G 67% T;T 3%

Other GP6 SNPs

All GP6 SNPs

Source and license

Adapted from rs1671152 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.