i6006915
From SNPedia
| 23andMe data | I6006915 |
| 23andMe search | I6006915 |
| opensnp | I6006915 |
| iGeno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | normal |
| (A;G) | 3 | carrier of a hypophosphatasia allele |
| (G;G) | 4 | hypophosphatasia |
i6006915, also known as c.883A>G or p.M295V, 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.
