ClinVar Miner

List of variants reported as uncertain significance for Atrial conduction disease by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015978.3(TNNI3K):c.1471C>T (p.Arg491Cys)	rs79936844	0.00004
NM_015978.3(TNNI3K):c.681T>C (p.Asp227=)	rs757108060	0.00004

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