ClinVar Miner

List of variants in gene TNNI3 reported as pathogenic by Stanford Center for Inherited Cardiovascular Disease, Stanford University

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.557G>A (p.Arg186Gln)	rs397516357	0.00001
NM_000363.5(TNNI3):c.610C>T (p.Arg204Cys)	rs727504243	0.00001

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