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


From SNPedia

23andMe dataI6006915
23andMe searchI6006915
iGeno Mag Summary
(A;A) 0 normal
(A;G) 3 carrier of a hypophosphatasia allele
(G;G) 4 hypophosphatasia

i6006915, also known as c.883A>G or p.M295V, 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 childhood form of hypophosphatasia.