List of variants in gene TNNI3 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn)	rs184709702	0.00006
NM_000363.5(TNNI3):c.372+7C>T	rs367809676	0.00004
NM_000363.5(TNNI3):c.283-9C>T	rs759922995	0.00002
NM_000363.5(TNNI3):c.322G>A (p.Asp108Asn)	rs766958196	0.00001
NM_000363.5(TNNI3):c.34C>T (p.Pro12Ser)	rs553214254	0.00001
NM_000363.5(TNNI3):c.373-17C>T	rs769481190	0.00001
NM_000363.5(TNNI3):c.550-12G>A	rs754944128	0.00001
NM_000363.5(TNNI3):c.632G>T (p.Ter211Leu)	rs730881084	0.00001
NM_000363.5(TNNI3):c.288G>C (p.Leu96Phe)	rs1599909725
NM_000363.5(TNNI3):c.298C>T (p.Leu100Phe)	rs773216333
NM_000363.5(TNNI3):c.511G>A (p.Ala171Thr)	rs121917761
NM_000363.5(TNNI3):c.549+68_549+69insGGCCTA	rs139158921
NM_000363.5(TNNI3):c.562G>A (p.Val188Met)	rs193922409
NM_000363.5(TNNI3):c.88G>A (p.Ala30Thr)	rs796104366

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