rs6413484
A SNP in the GHR gene on chromosome 5. Its most notable genotype is G;G: common in clinvar
- Gene
- GHR
- Location
- Chr 542,699,868 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- <1%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageG;G 0%
- European ancestry (Utah)G;G 0%
- Han Chinese (Beijing)G;G 0%
- Japanese (Tokyo)G;G 0%
- Yoruba (Nigeria)G;G 0%
Related
Other GHR SNPs
- rs121909363C;TCarrier of a Laron syndrome mutationImportant
- rs4590183C;Cd3/d3GHR homozygote; possibly longer longevity, at least in malesWorth knowing
- rs6873545C;Cd3/d3GHR homozygote; possibly longer longevity, at least in malesWorth knowing
- rs6180A;Acommon in clinvarTypical
- rs13188386G;GNo summary available.Typical
Source and license
Adapted from rs6413484 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.