rs2230600
A SNP in the PTPN13 gene on chromosome 4. Its most notable genotype is G;G.
- Gene
- PTPN13
- Location
- Chr 486,769,845 (GRCh38)
- Highest magnitude
- 1.9Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 19%
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 11 HapMap populations.
- AverageG;G 4%
- European ancestry (Utah)G;G 6%
- Han Chinese (Beijing)G;G 6%
- Japanese (Tokyo)G;G 12%
- Yoruba (Nigeria)G;G 0%
- African ancestry (Southwest US)G;G 0%
- Chinese (Denver)G;G 7%
- Gujarati IndianG;G 2%
- Luhya (Kenya)G;G 0%
- Mexican ancestry (Los Angeles)G;G 11%
- Maasai (Kenya)G;G 0%
- TuscanG;G 0%
Notes
From SNPedia
Notes
rs2230600 We found that a significantly increased squamous cell carcinoma of the head and neck risk was associated with the c.4566 I1522M (G;G) genotype [odds ratio (OR), 1.89; 95% confidence interval (CI), 1.27-2.79
Source and license
Adapted from rs2230600 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.