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i5900451

From SNPedia

23andMe dataI5900451
23andMe searchI5900451
opensnpI5900451
Gene (via rs)ALPL
iGeno Mag Summary
(C;C) 0 normal
(C;T) 3 carrier of a hypophosphatasia allele
(T;T) 4 hypophosphatasia

aliasrs121918015
Rs_StabilizedOrientationplus
RsGeno Mag Summary
(C;C) 0 normal
(C;T) 3 carrier of a hypophosphatasia allele
(T;T) 4 hypophosphatasia

i5900451, also known as c.323C>T or p.P108L, 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 odonto form of hypophosphatasia.