ClinVar Miner

List of variants reported as likely pathogenic for Atrial conduction disease

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_015978.3(TNNI3K):c.2302G>A (p.Glu768Lys)	rs202238194	0.00002
NM_015978.3(TNNI3K):c.2222C>A (p.Ser741Ter)	rs548261851
NM_015978.3(TNNI3K):c.538G>T (p.Glu180Ter)	rs746684996

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