Variants with conflicting interpretations "pathogenic" 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 "uncertain significance" 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: 6

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HGVS	dbSNP
NM_000527.4(LDLR):c.1186+5G>C	rs879254821
NM_000527.5(LDLR):c.1045C>T (p.Gln349Ter)	rs748300548
NM_000527.5(LDLR):c.1069G>A (p.Glu357Lys)	rs879254781
NM_000527.5(LDLR):c.1598G>A (p.Trp533Ter)	rs746939188
NM_000527.5(LDLR):c.941-12G>A	rs879254734
NM_174936.3(PCSK9):c.103G>T (p.Asp35Tyr)	rs764603059

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