rs876659610

A SNP in the MAX gene on chromosome 14. Its most notable genotype is A;T: Hereditary PGL/PCC Syndrome

Gene
MAX
Location
Chr 1465,077,996 (GRCh38)
Highest magnitude
6.2Very important
Tested on
AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. A;TMost notableBadHereditary PGL/PCC SyndromeVery important · 6.2
  2. A;AGoodcommon in clinvarTypical · 0.0

SNPedia records rs876659610 on the minus strand: (A;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Other MAX SNPs

All MAX SNPs

Source and license

Adapted from rs876659610 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.