List of variants in gene TNNT2 reported as likely pathogenic for Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.268C>A (p.Pro90Thr)	rs397516451
NM_001276345.2(TNNT2):c.311G>T (p.Arg104Leu)	rs397516457
NM_001276345.2(TNNT2):c.430C>T (p.Arg144Trp)	rs45525839
NM_001276345.2(TNNT2):c.863G>C (p.Arg288Pro)	rs397516484

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