rs4902359
A SNP in the MAX gene on chromosome 14. Its most notable genotype is G;G: common in clinvar
- Gene
- MAX
- Location
- Chr 1465,076,072 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 46%
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 29%
- European ancestry (Utah)G;G 45%
- Han Chinese (Beijing)G;G 43%
- Japanese (Tokyo)G;G 20%
- Yoruba (Nigeria)G;G 1%
- African ancestry (Southwest US)G;G 4%
- Chinese (Denver)G;G 39%
- Gujarati IndianG;G 39%
- Luhya (Kenya)G;G 7%
- Mexican ancestry (Los Angeles)G;G 68%
- Maasai (Kenya)G;G 9%
- TuscanG;G 43%
Related
Other MAX SNPs
- rs387906650A;GHereditary PGL/PCC SyndromeVery important
- rs786203009A;THereditary PGL/PCC SyndromeVery important
- rs786203385C;THereditary PGL/PCC SyndromeVery important
- rs876659610A;THereditary PGL/PCC SyndromeVery important
- rs876660073G;THereditary PGL/PCC SyndromeVery important
- rs1957948C;Ccommon in clinvarTypical
- rs1957949C;Ccommon in clinvarTypical
Source and license
Adapted from rs4902359 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.