rs387906503(-;-)
From SNPedia
| deletion variant of uncertain significance |
| Is a | genotype |
| of | rs387906503 |
| Gene | AGTR2 |
| Chromosome | X |
| Position | 116,172,682 |
| mentioned | by |
| Magnitude | 1 |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 1 | deletion variant of uncertain significance |
| (-;T) | 1 | deletion variant of uncertain significance |
| (T;T) | 0 | common in clinvar |
see rs387906503
