| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | GPR150, LOC123497940 (A269T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GPR150, LOC123497940 (G332S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GPR150, LOC123497940 (R361Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GPR150, LOC123497940 (L370R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GPR150, LOC123497940 (G371C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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