| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC125418060, MRAP
+1 more (V39M) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | LOC125418060, MRAP
+1 more (W43L) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC125418060, MRAP
+1 more (M1I +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC125418060, MRAP
+1 more (A5T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC125418060, MRAP
+1 more (S65F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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