| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | MYH11, NDE1 (E1833D +1 more) | Single nucleotide variant (missense variant +1 more) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | See cases +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | GConflicting classifications of pathogenicity |
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