| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130004317, PANK1 +1 more (A18S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130004317, PANK1 +1 more | Single nucleotide variant (5 prime UTR variant) | Inborn genetic diseases | |
| | LOC130004317, PANK1 +1 more | Single nucleotide variant (5 prime UTR variant) | Inborn genetic diseases | |
Click to view in NCBI Gene