| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | JMJD7, JMJD7-PLA2G4B +1 more (P17L) | Single nucleotide variant (missense variant) | not provided | |
| | JMJD7, JMJD7-PLA2G4B (A28G) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Duplication | Familial colorectal cancer +1 more | |
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