Have questions? Visit https://www.reddit.com/r/SNPedia

i6006936

From SNPedia

23andMe dataI6006936
23andMe searchI6006936
opensnpI6006936
iGeno Mag Summary
(G;G) 0 normal
(G;T) 3 carrier of a hypophosphatasia allele
(T;T) 4 hypophosphatasia

i6006936, also known as c.871G>T or p.E291X, is a SNP in the ALPL gene on chromosome 1. Based on the ALPL gene mutations database, the rare/minor allele is considered pathogenic for the perinatal form of hypophosphatasia.