rs775863165(C;T)
From SNPedia
| Carrier of a mutation in the HPCA gene, but significance unclear |
| Is a | genotype |
| of | rs775863165 |
| Gene | HPCA |
| Chromosome | 1 |
| Position | 32,889,110 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 5.7 | Dystonia 2, torsion (DYT2) genotype |
| (A;C) | 3 | Carrier of a dystonia (DYT2) mutation |
| (C;C) | 0 | common in clinvar |
| (C;T) | 3 | Carrier of a mutation in the HPCA gene, but significance unclear |
see rs775863165
