| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | GEMIN7, LOC130064668 +1 more (I32M) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | GEMIN7, LOC130064668 +1 more (M25L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | GEMIN7, LOC130064668 +1 more (E14Q) | Single nucleotide variant (missense variant +1 more) | not specified | |
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