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From SNPedia
23andMe dataI6007020
23andMe searchI6007020
iGeno Mag Summary
(G;G) 4 hypophosphatasia
(G;T) 3 carrier of a hypophosphatasia allele
(T;T) 0 normal

i6007020, also known as c.889T>G or p.Y297D, 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.