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

i6006901

From SNPedia
23andMe dataI6006901
23andMe searchI6006901
opensnpI6006901
iGeno Mag Summary
(C;C) 4 hypophosphatasia
(C;T) 3 carrier of a hypophosphatasia allele
(T;T) 0 normal

i6006901, also known as c.1064T>C or p.M355T, 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.