Variants with conflicting interpretations "benign" from Stanford Center for Inherited Cardiovascular Disease, Stanford University and "uncertain significance" from any submitter

Minimum review status of the submission from Stanford Center for Inherited Cardiovascular Disease, Stanford University:		Collection method of the submission from Stanford Center for Inherited Cardiovascular Disease, Stanford University:
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_001032283.3(TMPO):c.565+2487C>T	rs17028450	0.00576
NM_002294.3(LAMP2):c.1093+2514G>A	rs144140265	0.00404
NM_174934.4(SCN4B):c.22G>A (p.Gly8Ser)	rs149868494	0.00009
NM_000335.5(SCN5A):c.52C>T (p.Arg18Trp)	rs199473044	0.00006
NM_004415.4(DSP):c.4741A>G (p.Lys1581Glu)	rs186842903	0.00003

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