ClinVar Miner

List of variants in gene combination ATP6V0E1, BNIP1, CREBRF, DUSP1, ERGIC1, NEURL1B, NKX2-5, RPL26L1, SNORA74B, STC2 reported as pathogenic for atrial septal defect 7

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NC_000005.9:g.(?_172089144)_(172774583_?)del

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