Variants with conflicting interpretations "uncertain significance" from Centre de Génétique Moléculaire et Chromosomique, Unité de génétique de l'Obésité et des Dyslipidémies,APHP, GH Hôpitaux Universitaires Pitié-Salpêtrière / Charles-Foix and "likely benign" from any submitter

Minimum review status of the submission from Centre de Génétique Moléculaire et Chromosomique, Unité de génétique de l'Obésité et des Dyslipidémies,APHP, GH Hôpitaux Universitaires Pitié-Salpêtrière / Charles-Foix:		Collection method of the submission from Centre de Génétique Moléculaire et Chromosomique, Unité de génétique de l'Obésité et des Dyslipidémies,APHP, GH Hôpitaux Universitaires Pitié-Salpêtrière / Charles-Foix:
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
NM_000527.4(LDLR):c.1158C>G (p.Asp386Glu)	rs879254810
NM_000527.4(LDLR):c.1358+7G>A	rs369709333
NM_000527.4(LDLR):c.1510A>G (p.Lys504Glu)	rs730882103
NM_000527.4(LDLR):c.2282C>T (p.Thr761Met)	rs138477254
NM_000527.4(LDLR):c.2548-12A>G	rs771336748
NM_174936.3(PCSK9):c.1274A>G (p.Asn425Ser)	rs28362261
NM_174936.3(PCSK9):c.709C>T (p.Arg237Trp)	rs148195424
NM_174936.3(PCSK9):c.835C>A (p.Pro279Thr)	rs72646509

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