ClinVar Miner

List of variants reported as uncertain significance for Atrial conduction disease by Molecular Genetics, Royal Melbourne Hospital

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015978.3(TNNI3K):c.19A>G (p.Arg7Gly)	rs2524304033	0.00001
NM_015978.3(TNNI3K):c.380T>C (p.Ile127Thr)	rs779098224	0.00001

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