rs786203385
A SNP in the MAX gene on chromosome 14. Its most notable genotype is C;T: Hereditary PGL/PCC Syndrome
- Gene
- MAX
- Location
- Chr 1465,077,912 (GRCh38)
- Highest magnitude
- 6.2Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- C;TMost notableBadHereditary PGL/PCC Syndrome
- C;CGoodcommon in clinvar
SNPedia records rs786203385 on the minus strand: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other MAX SNPs
- rs387906650A;GHereditary PGL/PCC SyndromeVery important
- rs786203009A;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
- rs4902359G;Gcommon in clinvarTypical
Source and license
Adapted from rs786203385 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.