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

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.1805C>T (p.Thr602Ile)	rs730880551	0.00001
NM_000363.5(TNNI3):c.428C>A (p.Thr143Asn)	rs397516348	0.00001
NM_001005242.3(PKP2):c.2261_2269del (p.Thr754_Asn756del)	rs1270283587
NM_001267550.2(TTN):c.4714C>T (p.Arg1572Ter)	rs1554008881
NM_144573.4(NEXN):c.1878dup (p.Asp627fs)	rs2102181621

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