| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130057313, PDCD7 (Y81H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130057313, PDCD7 (R65G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130057313, PDCD7 (A61T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130057313, PDCD7 (P59L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130057313, PDCD7 (P54A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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