| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126859666, RNF8 (N281D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126859666, RNF8 (L299V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126859666, RNF8 (Q303R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126859666, RNF8 (G217R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126859666, RNF8 (T198I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126859666, RNF8 (S157N) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126859666, RNF8 (L136V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126859666, RNF8 (N202S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126859666, RNF8 (I132V) | Single nucleotide variant (missense variant +1 more) | not specified | |
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