| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | DNMT3B, LOC126863014 (P467L +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | DNMT3B, LOC126863014 (R511C +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | DNMT3B, LOC126863014 (R531H +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LOC126863014, DNMT3B (R475W +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | DNMT3B, LOC126863014 (G547V +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | DNMT3B, LOC126863014 (A473T +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene