| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126862647, RNF157 (V178M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862647, RNF157 (S158L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862647, RNF157 (D153H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862647, RNF157 (V130I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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