ClinVar Miner

List of variants in gene COX7B reported as pathogenic for X-linked syndromic intellectual disability

Included ClinVar conditions (163):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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NM_001866.2(COX7B):c.196del (p.Leu66Cysfs) rs397514583
NM_001866.2(COX7B):c.55C>T (p.Gln19Ter) rs397514585
NM_001866.3(COX7B):c.41-2A>G rs397514584

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