rs779709646(C;T)
From SNPedia
Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
Is a | genotype |
of | rs779709646 |
Gene | DHCR7 |
Chromosome | 11 |
Position | 71,435,664 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 3 | Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation |
(T;T) | 9 | Smith-Lemli-Opitz syndrome |