| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862867, ADGRE5 (P170L) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADGRE5, LOC126862867 (V181L) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADGRE5, LOC126862867 (P190L) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126862867, ADGRE5 (V206I) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
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