rs1130495

A SNP in the PTPRN2 gene on chromosome 7. Its most notable genotype is G;G: common on affy axiom data

Gene
PTPRN2
Location
Chr 7158,167,219 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
11%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon on affy axiom dataTypical · 0.076% of people
  2. C;CNot ratedNo summary available.Typical · 0.00% of people

SNPedia records rs1130495 on the minus strand: (C;C), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 9 HapMap populations.

  • AverageG;G 76% C;C 0%
  • European ancestry (Utah)G;G 76% C;C 0%
  • Han Chinese (Beijing)G;G 78% C;C 0%
  • Japanese (Tokyo)G;G 73% C;C 0%
  • Yoruba (Nigeria)G;G 78% C;C 0%
  • African ancestry (Southwest US)G;G 74% C;C 0%
  • Chinese (Denver)G;G 82% C;C 0%
  • Gujarati IndianG;G 65% C;C 0%
  • Luhya (Kenya)G;G 82% C;C 0%
  • TuscanG;G 73% C;C 0%

Source and license

Adapted from rs1130495 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.