rs797044948(A;G)
From SNPedia
| Reported to be an inborn genetic disease (of unspecified type) |
| Is a | genotype |
| of | rs797044948 |
| Gene | VPS35 |
| Chromosome | 16 |
| Position | 46,671,766 |
| mentioned | by |
| Magnitude | 4.4 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;G) | 4.4 | Reported to be an inborn genetic disease (of unspecified type) |
see rs797044948
