Variants with conflicting interpretations "benign" from Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute and "uncertain significance" from Eurofins Ntd Llc (ga)

Minimum review status of the submission from Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute:		Collection method of the submission from Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute:
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: 4

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HGVS	dbSNP	gnomAD frequency
NM_022437.3(ABCG8):c.1201A>T (p.Thr401Ser)	rs144200355	0.00179
NM_000257.4(MYH7):c.2769C>T (p.Asn923=)	rs36211716	0.00060
NM_000719.7(CACNA1C):c.2280G>A (p.Glu760=)	rs141633456	0.00025
NM_001035.3(RYR2):c.5712G>A (p.Leu1904=)	rs377763336	0.00001

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