| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC105375131, SDK1 (V1330M) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | LOC105375131, SDK1 (V1347M) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | LOC105375131, SDK1 (V1385L) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC105375131, SDK1 (T1392I) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene