Variants in gene TNNT2 with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys)	rs121964857	0.00044
NM_001276345.2(TNNT2):c.460C>T (p.Arg154Trp)	rs483352832	0.00003
NM_001276345.2(TNNT2):c.277G>A (p.Glu93Lys)	rs727504244	0.00001
NM_001276345.2(TNNT2):c.321G>T (p.Lys107Asn)	rs397516459
NM_001276345.2(TNNT2):c.446G>A (p.Arg149His)	rs397516466
NM_001276345.2(TNNT2):c.643C>T (p.Arg215Trp)	rs45586240
NM_001276345.2(TNNT2):c.644G>A (p.Arg215Gln)	rs121964860
NM_001276345.2(TNNT2):c.838G>A (p.Asp280Asn)	rs121964861
NM_001276345.2(TNNT2):c.844C>T (p.Gln282Ter)	rs796925245
NM_001276345.2(TNNT2):c.852-2A>C	rs111692981

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