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

i6006908

From SNPedia

23andMe dataI6006908
23andMe searchI6006908
opensnpI6006908
iGeno Mag Summary
(A;A) 0 normal
(A;G) 3 carrier of a hypophosphatasia allele
(G;G) 4 hypophosphatasia

i6006908, also known as c.442A>G or p.T148A, 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.