Variants with conflicting interpretations "pathogenic" from Klaassen Lab, Charite University Medicine Berlin and "uncertain significance" from any submitter

Minimum review status of the submission from Klaassen Lab, Charite University Medicine Berlin:		Collection method of the submission from Klaassen Lab, Charite University Medicine Berlin:
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_001276345.2(TNNT2):c.460C>T (p.Arg154Trp)	rs483352832	0.00003
NM_001103.4(ACTN2):c.574C>T (p.Arg192Ter)	rs1253211384	0.00001
NM_000256.3(MYBPC3):c.709T>C (p.Tyr237His)	rs730880624

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