| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129929222, RNF207 (S2W) | Single nucleotide variant (missense variant) | not specified | |
| | LOC121967057, RNF207 (C119Y) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (splice donor variant) | Long QT syndrome | |
Click to view in NCBI Gene