ClinVar Miner

List of variants reported as likely pathogenic for dextrocardia

Included ClinVar conditions (2):

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_145020.5(CFAP53):c.472A>G (p.Arg158Gly)	rs886037751	0.00001
NM_001127392.3(MYRF):c.1786C>T (p.Gln596Ter)	rs762143393
NM_145020.5(CFAP53):c.301_473+1del	rs1555672928

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