Variants with conflicting interpretations "likely benign" from Illumina Laboratory Services, Illumina and "association" from any submitter

Minimum review status of the submission from Illumina Laboratory Services, Illumina:		Collection method of the submission from Illumina Laboratory Services, Illumina:
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_000207.3(INS):c.*9C>T	rs3842752	0.16663
NM_174936.4(PCSK9):c.426C>G (p.Tyr142Ter)	rs67608943	0.00048
NM_174936.4(PCSK9):c.137G>T (p.Arg46Leu)

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