List of variants in gene TNNI3 reported as uncertain significance for Cardiovascular phenotype

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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: 10

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HGVS	dbSNP
NM_000363.5(TNNI3):c.143A>C (p.Gln48Pro)	rs200720341
NM_000363.5(TNNI3):c.173A>G (p.Lys58Arg)	rs878853955
NM_000363.5(TNNI3):c.221G>C (p.Arg74Pro)	rs886039022
NM_000363.5(TNNI3):c.250G>T (p.Glu84Ter)	rs759523214
NM_000363.5(TNNI3):c.308G>A (p.Arg103His)	rs371000425
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn)	rs184709702
NM_000363.5(TNNI3):c.539A>G (p.Asp180Gly)	rs1060499912
NM_000363.5(TNNI3):c.581A>C (p.Asn194Thr)	rs730881081
NM_000363.5(TNNI3):c.614A>C (p.Lys205Thr)	rs1555862962
NM_000363.5(TNNI3):c.88G>A (p.Ala30Thr)	rs796104366

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