ClinVar Miner

List of variants in gene KAT6A reported as likely benign for autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP
NM_006766.5(KAT6A):c.2983G>A (p.Glu995Lys) rs779315883
NM_006766.5(KAT6A):c.5525C>G (p.Thr1842Arg) rs886037914

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