Variants in gene TNNI3 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 15

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.422G>A (p.Arg141Gln)	rs397516347	0.00004
NM_000363.5(TNNI3):c.484C>T (p.Arg162Trp)	rs368861241	0.00004
NM_000363.5(TNNI3):c.434G>A (p.Arg145Gln)	rs397516349	0.00002
NM_000363.5(TNNI3):c.433C>T (p.Arg145Trp)	rs104894724	0.00001
NM_000363.5(TNNI3):c.485G>A (p.Arg162Gln)	rs397516354	0.00001
NM_000363.5(TNNI3):c.497C>T (p.Ser166Phe)	rs727504242	0.00001
NM_000363.5(TNNI3):c.557G>A (p.Arg186Gln)	rs397516357	0.00001
NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn)	rs104894727	0.00001
NM_000363.5(TNNI3):c.204del (p.Arg69fs)	rs727504872
NM_000363.5(TNNI3):c.470C>T (p.Ala157Val)	rs397516353
NM_000363.5(TNNI3):c.485G>C (p.Arg162Pro)	rs397516354
NM_000363.5(TNNI3):c.509G>A (p.Arg170Gln)	rs727503503
NM_000363.5(TNNI3):c.523C>T (p.Gln175Ter)	rs876661394
NM_000363.5(TNNI3):c.544G>A (p.Glu182Lys)	rs397516355
NM_000363.5(TNNI3):c.611G>A (p.Arg204His)	rs727504275

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