List of variants in gene TNNT2 reported as uncertain significance 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.436G>A (p.Glu146Lys)	rs371142225	0.00001
NM_001276345.2(TNNT2):c.430C>T (p.Arg144Trp)	rs45525839
NM_001276345.2(TNNT2):c.487G>A (p.Ala163Thr)	rs727505030
NM_001276345.2(TNNT2):c.547C>G (p.Arg183Gly)	rs727503512
NM_001276345.2(TNNT2):c.572T>G (p.Met191Arg)	rs869025538
NM_001276345.2(TNNT2):c.651G>C (p.Lys217Asn)	rs1571605501
NM_001276345.2(TNNT2):c.808G>A (p.Glu270Lys)	rs1131691898
NM_001276345.2(TNNT2):c.817G>A (p.Val273Ile)	rs1571590208

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