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 pathogenic" 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: 15

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HGVS	dbSNP
NM_000527.5(LDLR):c.1166C>T (p.Thr389Met)	rs149227308
NM_000527.5(LDLR):c.1201C>G (p.Leu401Val)
NM_000527.5(LDLR):c.1217G>A (p.Arg406Gln)	rs552422789
NM_000527.5(LDLR):c.1238C>T (p.Thr413Met)	rs368562025
NM_000527.5(LDLR):c.139G>A (p.Asp47Asn)
NM_000527.5(LDLR):c.1432G>A (p.Gly478Arg)
NM_000527.5(LDLR):c.1586+5G>A	rs781362878
NM_000527.5(LDLR):c.1720C>T (p.Arg574Cys)	rs185098634
NM_000527.5(LDLR):c.1855T>C (p.Phe619Leu)	rs747134711
NM_000527.5(LDLR):c.2215C>T (p.Gln739Ter)	rs370018159
NM_000527.5(LDLR):c.2416dup (p.Val806fs)
NM_000527.5(LDLR):c.343C>T (p.Arg115Cys)	rs774723292
NM_000527.5(LDLR):c.352G>T (p.Asp118Tyr)	rs730882080
NM_000527.5(LDLR):c.664T>C (p.Cys222Arg)	rs577934998
NM_000527.5(LDLR):c.862G>A (p.Glu288Lys)	rs368657165

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