| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130062794, TXNL4A (S2L) | Single nucleotide variant (5 prime UTR variant +3 more) | Inborn genetic diseases | |
Click to view in NCBI Gene