List of variants in gene TNNT2 reported as likely pathogenic for Primary dilated cardiomyopathy

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

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.544G>T (p.Ala182Ser)	rs730881097	0.00002
NM_001276345.2(TNNT2):c.452G>A (p.Arg151Gln)	rs730881101	0.00001
NM_001276345.2(TNNT2):c.275G>A (p.Gly92Glu)
NM_001276345.2(TNNT2):c.294T>A (p.Asp98Glu)	rs397516454
NM_001276345.2(TNNT2):c.294T>G (p.Asp98Glu)	rs397516454
NM_001276345.2(TNNT2):c.354_355delinsGT (p.His119Tyr)	rs876658027
NM_001276345.2(TNNT2):c.382G>A (p.Glu128Lys)	rs397516461
NM_001276345.2(TNNT2):c.421C>T (p.Arg141Trp)	rs74315380
NM_001276345.2(TNNT2):c.422G>C (p.Arg141Pro)	rs397516464
NM_001276345.2(TNNT2):c.430C>G (p.Arg144Gly)	rs45525839
NM_001276345.2(TNNT2):c.446G>A (p.Arg149His)	rs397516466
NM_001276345.2(TNNT2):c.481C>T (p.Arg161Cys)	rs45608937
NM_001276345.2(TNNT2):c.548G>A (p.Arg183Gln)	rs397516471
NM_001276345.2(TNNT2):c.630G>C (p.Lys210Asn)
NM_001276345.2(TNNT2):c.643C>T (p.Arg215Trp)	rs45586240
NM_001276345.2(TNNT2):c.650AGA[3] (p.Lys220del)	rs45578238
NM_001276345.2(TNNT2):c.652A>G (p.Lys218Glu)

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