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

i6007008

From SNPedia

23andMe dataI6007008
23andMe searchI6007008
opensnpI6007008
iGeno Mag Summary
(G;G) 0 normal
(G;T) 3 carrier of a hypophosphatasia allele
(T;T) 4 hypophosphatasia

i6007008, also known as c.151G>T or p.A51S, 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 infantile form of hypophosphatasia.