List of variants in gene TNNT2 reported as benign by Color Diagnostics, LLC DBA Color Health

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.348C>T (p.Ile116=)	rs3729547	0.69444
NM_001276345.2(TNNT2):c.237G>A (p.Ser79=)	rs3729845	0.08311
NM_001276345.2(TNNT2):c.788A>G (p.Lys263Arg)	rs3730238	0.05965
NM_001276345.2(TNNT2):c.610-90G>A	rs11810834	0.03251
NM_001276345.2(TNNT2):c.68-8A>G	rs115805892	0.00864
NM_001276345.2(TNNT2):c.474G>C (p.Arg158=)	rs35914325	0.00788
NM_001276345.2(TNNT2):c.610-106C>T	rs373805222	0.00113
NM_001276345.2(TNNT2):c.200-11A>G	rs368658464	0.00021
NM_001276345.2(TNNT2):c.601-8C>T	rs397516475	0.00006
NM_001276345.2(TNNT2):c.522C>T (p.Asn174=)	rs483352833	0.00001
NM_001276345.2(TNNT2):c.412-6_412-4del	rs397516462
NM_001276345.2(TNNT2):c.53-11_53-7del	rs45533739

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