i6007019
From SNPedia
| 23andMe data | I6007019 |
| 23andMe search | I6007019 |
| opensnp | I6007019 |
| iGeno | Mag | Summary |
|---|---|---|
| (A;A) | 4 | hypophosphatasia |
| (A;G) | 3 | carrier of a hypophosphatasia allele |
| (G;G) | 0 | normal |
i6007019, also known as c.1270G>A or p.V424M, 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 adult form of hypophosphatasia.
