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From SNPedia

23andMe dataI6006988
23andMe searchI6006988
iGeno Mag Summary
(C;C) 0 normal
(C;G) 3 carrier of a hypophosphatasia allele
(G;G) 4 hypophosphatasia

i6006988, also known as c.341C>G or p.A114G, 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.