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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 13

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HGVS	dbSNP	gnomAD frequency
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.372+7C>T	rs367809676	0.00004
NM_000363.5(TNNI3):c.-8G>A	rs773513015	0.00003
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr)	rs374618872	0.00003
NM_000363.5(TNNI3):c.45A>C (p.Ala15=)	rs377421427	0.00003
NM_000363.5(TNNI3):c.151-6C>G	rs377258542	0.00002
NM_000363.5(TNNI3):c.340A>G (p.Ile114Val)	rs730881070	0.00001
NM_000363.5(TNNI3):c.384G>A (p.Leu128=)	rs373130533	0.00001
NM_000363.5(TNNI3):c.55A>G (p.Ile19Val)	rs755862334	0.00001
NM_000363.5(TNNI3):c.12-7del	rs370714315
NM_000363.5(TNNI3):c.157C>T (p.Leu53=)	rs763981651
NM_000363.5(TNNI3):c.25-7A>C	rs1171407156

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