| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | LOC130009247, NOC4L (A13G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130009247, NOC4L (R16G) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
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