| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ASNS, CZ1P-ASNS (S480F +2 more) | Single nucleotide variant (missense variant +1 more) | Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
Click to view in NCBI Gene