| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862088, TRPM1 (F1167L +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | LOC126862088, TRPM1 (S1115I +2 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC126862088, TRPM1 (P1132R +2 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC126862088, TRPM1 (H1124N +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene