i6006952
From SNPedia
23andMe data | I6006952 |
23andMe search | I6006952 |
opensnp | I6006952 |
iGeno | Mag | Summary |
---|---|---|
(A;A) | 4 | hypophosphatasia |
(A;G) | 3 | carrier of a hypophosphatasia allele |
(G;G) | 0 | normal |
i6006952, also known as c.334G>A or p.G112S, 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 infantile form of hypophosphatasia.