Variants in gene TNNI3 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.-85A>C	rs186540595	0.00142
NM_000363.5(TNNI3):c.-103C>T	rs557391836	0.00102
NM_000363.5(TNNI3):c.373-4C>G	rs2288530	0.00007
NM_000363.5(TNNI3):c.139T>C (p.Leu47=)	rs587780967	0.00006
NM_000363.5(TNNI3):c.151-6C>G	rs377258542	0.00002
NM_000363.5(TNNI3):c.12-7del	rs370714315
NM_000363.5(TNNI3):c.173A>G (p.Lys58Arg)	rs878853955

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