Variants with conflicting interpretations "pathogenic" from KTest Genetics, KTest and "likely pathogenic" from any submitter

Minimum review status of the submission from KTest Genetics, KTest:		Collection method of the submission from KTest Genetics, KTest:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_001134363.3(RBM20):c.1907G>A (p.Arg636His)	rs267607004	0.00001
NM_001276345.2(TNNT2):c.548G>A (p.Arg183Gln)	rs397516471
NM_001276345.2(TNNT2):c.650AGA[3] (p.Lys220del)	rs45578238

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