| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | SARM1, SLC46A1 (T377M +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Congenital defect of folate absorption +1 more | GConflicting classifications of pathogenicity |
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