Variants with conflicting interpretations "likely 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 "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: 11

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HGVS	dbSNP
NM_000527.5(LDLR):c.1060+10G>A
NM_000527.5(LDLR):c.1153C>G (p.Leu385Val)	rs879254808
NM_000527.5(LDLR):c.1288G>C (p.Val430Leu)	rs879254853
NM_000527.5(LDLR):c.1495T>C (p.Ser499Pro)	rs879254921
NM_000527.5(LDLR):c.1928C>T (p.Ala643Val)	rs879255075
NM_000527.5(LDLR):c.1975A>C (p.Thr659Pro)	rs773693079
NM_000527.5(LDLR):c.226G>T (p.Gly76Trp)	rs574337291
NM_000527.5(LDLR):c.2547+5G>C	rs879255226
NM_000527.5(LDLR):c.598T>A (p.Phe200Ile)	rs879254585
NM_000527.5(LDLR):c.798T>A (p.Asp266Glu)	rs139043155
NM_000527.5(LDLR):c.932A>G (p.Lys311Arg)	rs761765254

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