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

i5002770

From SNPedia

23andMe dataI5002770
23andMe searchI5002770
opensnpI5002770
Gene (via rs)ALPL
GeneALPL
Chromosome1
Position21887155
iGeno Mag Summary
(C;C) 0 normal
(C;T) 3 carrier of a hypophosphatasia allele
(T;T) 4 hypophosphatasia

aliasrs121918005
Rs_StabilizedOrientationplus
RsGeno Mag Summary
(C;C) 0 normal
(C;T) 3 carrier of a hypophosphatasia allele
(T;T) 4 hypophosphatasia

i5002770, also known as c.98C>T or p.A33V, 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.