rs397514442(-;CT)
From SNPedia
| Likely miscall in Ancestry v2c data; otherwise, carrier of a bile acid synthesis defect mutation |
| Is a | genotype |
| of | rs397514442 |
| Gene | HSD3B7 |
| Chromosome | 16 |
| Position | 30,988,112 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (-;CT) | 3 | Likely miscall in Ancestry v2c data; otherwise, carrier of a bile acid synthesis defect mutation |
| (CT;CT) | 0 | common in clinvar |
Unaffected in absence of a second mutation in the HSD3B7 gene; see links via main rs-page.
