Links from MedGen
Items: 14
| Variation | | Type (Consequence) | Condition | Classification, Review status |
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| | | Deletion (frameshift variant) | Microcephaly and chorioretinopathy 2 | |
| | | Deletion (frameshift variant) | Microcephaly and chorioretinopathy 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Microcephaly and chorioretinopathy 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly and chorioretinopathy 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly and chorioretinopathy 2 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Microcephaly and chorioretinopathy 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly and chorioretinopathy 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Microcephaly and chorioretinopathy 2 | |
| | | Single nucleotide variant (splice donor variant) | Microcephaly and chorioretinopathy 2 | |
| | | Single nucleotide variant (intron variant) | Microcephaly and chorioretinopathy 2 +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | PLK4-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Microcephaly and chorioretinopathy 2 | |
Click to view in NCBI Gene