rs143312232(C;G)
From SNPedia
| Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
| Is a | genotype |
| of | rs143312232 |
| Gene | DHCR7 |
| Chromosome | 11 |
| Position | 71,441,392 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;C) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
| (C;G) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
| (G;G) | 0 | common in clinvar |
