Links from MedGen
Items: 6
| Variation | | Type (Consequence) | Condition | Classification, Review status |
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| | | Deletion (inframe deletion) | Microcephaly 27, primary, autosomal dominant | |
| | | Single nucleotide variant (missense variant) | Microcephaly 27, primary, autosomal dominant | |
| | | Single nucleotide variant (missense variant) | Microcephaly 27, primary, autosomal dominant +1 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly 27, primary, autosomal dominant | |
| | | Single nucleotide variant (missense variant) | LMNB2-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +4 more | |
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