| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (synonymous variant) | TOR1AIP1-related disorder | |
| | LOC112577517, TOR1AIP1 (P24A) | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy type 2Y +3 more | GConflicting classifications of pathogenicity |
| | LOC112577517, TOR1AIP1 (M146T) | Single nucleotide variant (missense variant) | not specified +2 more | |
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