| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC105369149, SBF2
+1 more (I1789V +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | LOC105369149, SBF2
+1 more (Y1733C +2 more) | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 4B2 +1 more | |
| | LOC105369149, SBF2
+1 more (S1685W +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | SBF2-AS1, LOC105369149
+1 more (K1602R +2 more) | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 4 +4 more | |
Click to view in NCBI Gene