Variants with conflicting interpretations "benign" from Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute and "likely benign" from ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.4455G>T (p.Arg1485Ser)	rs113902911	0.00572
NM_014391.3(ANKRD1):c.319G>T (p.Val107Leu)	rs114435632	0.00269
NM_004415.4(DSP):c.1206G>A (p.Lys402=)	rs150422458	0.00185
NM_004415.4(DSP):c.741G>A (p.Ala247=)	rs2806234	0.00083
NM_004415.4(DSP):c.4065T>C (p.Tyr1355=)	rs148478829	0.00073
NM_000371.4(TTR):c.328C>A (p.His110Asn)	rs121918074	0.00040
NM_000238.4(KCNH2):c.551GCGCGGGCG[1] (p.184GAG[1])	rs551056698
NM_000384.3(APOB):c.10780T>C (p.Trp3594Arg)

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