Variants with conflicting interpretations "uncertain significance" from Klaassen Lab, Charite University Medicine Berlin and "likely benign" 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_001318895.3(FHL2):c.337C>T (p.Arg113Cys)	rs140148322	0.00036
NM_033118.4(MYLK2):c.425G>T (p.Gly142Val)	rs56385445	0.00006
NM_004415.4(DSP):c.4961T>C (p.Leu1654Pro)	rs749730642	0.00001

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