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

i6007036

From SNPedia

23andMe dataI6007036
23andMe searchI6007036
opensnpI6007036
iGeno Mag Summary
(A;A) 4 hypophosphatasia
(A;T) 3 carrier of a hypophosphatasia allele
(T;T) 0 normal

i6007036, also known as c.17T>A or p.L6X, 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.