rs138659167(A;C)
From SNPedia
| Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
| Is a | genotype |
| of | rs138659167 |
| Gene | DHCR7 |
| Chromosome | 11 |
| Position | 71,435,840 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;C) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
| (C;C) | 0 | common in clinvar |
| (C;G) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
