| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CYP7A1, LOC110596866 (A13V) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | CYP7A1, LOC110596866 (G9R) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | CYP7A1, LOC110596866 (W8C) | Single nucleotide variant (missense variant) | CYP7A1-related disorder | |
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