ClinVar Miner

List of variants reported as pathogenic for atrial septal defect 7 by Center for Medical Genetics Ghent, University of Ghent

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_004387.4(NKX2-5):c.768T>G (p.Tyr256Ter) rs104893907

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