List of variants in gene TNNT2 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.811-122C>G	rs45509695	0.22049
NM_001276345.2(TNNT2):c.163+12G>A	rs45580032	0.01441
NM_001276345.2(TNNT2):c.42-20G>A	rs45561443	0.01192
NM_001276345.2(TNNT2):c.294+7G>A	rs45490292	0.01066
NM_001276345.2(TNNT2):c.68-8A>G	rs115805892	0.00864
NM_001276345.2(TNNT2):c.610-81C>T	rs28730745	0.00831
NM_001276345.2(TNNT2):c.474G>C (p.Arg158=)	rs35914325	0.00788
NM_001276345.2(TNNT2):c.68-3del	rs200153031	0.00133
NM_001276345.2(TNNT2):c.68-5C>T	rs540630390	0.00133
NM_001276345.2(TNNT2):c.98-81G>A	rs45576939	0.00067
NM_001276345.2(TNNT2):c.53-11_53-7del	rs45533739

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