rs6180

A SNP in the GHR gene on chromosome 5. Its most notable genotype is A;A: common in clinvar

Gene
GHR
Location
Chr 542,719,137 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
44%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in clinvarTypical · 0.029% of people
  2. C;CNot ratedNo summary available.Typical · 0.022% of people

On SNPedia: (A;A), (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.

  • AverageA;A 29% C;C 22%
  • European ancestry (Utah)A;A 27% C;C 18%
  • Han Chinese (Beijing)A;A 10% C;C 34%
  • Japanese (Tokyo)A;A 20% C;C 33%
  • Yoruba (Nigeria)A;A 33% C;C 18%
  • African ancestry (Southwest US)A;A 49% C;C 7%
  • Chinese (Denver)A;A 7% C;C 40%
  • Gujarati IndianA;A 33% C;C 20%
  • Luhya (Kenya)A;A 44% C;C 9%
  • Mexican ancestry (Los Angeles)A;A 31% C;C 17%
  • Maasai (Kenya)A;A 34% C;C 19%
  • TuscanA;A 25% C;C 28%

Other GHR SNPs

All GHR SNPs

Source and license

Adapted from rs6180 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.