Variants with conflicting interpretations "pathogenic" from Women's Health and Genetics/Laboratory Corporation of America, LabCorp and "likely pathogenic" from Cardiovascular Research Group, Instituto Nacional de Saude Doutor Ricardo Jorge

Minimum review status of the submission from Women's Health and Genetics/Laboratory Corporation of America, LabCorp:		Collection method of the submission from Women's Health and Genetics/Laboratory Corporation of America, LabCorp:
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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.910G>A (p.Asp304Asn)	rs121908030	0.00006
NM_000527.5(LDLR):c.798T>A (p.Asp266Glu)	rs139043155	0.00004
NM_000527.5(LDLR):c.862G>A (p.Glu288Lys)	rs368657165	0.00003
NM_000527.5(LDLR):c.268G>A (p.Asp90Asn)	rs749038326	0.00002
NM_000527.5(LDLR):c.1222G>A (p.Glu408Lys)	rs137943601	0.00001
NM_000527.5(LDLR):c.190+4A>T	rs769446356	0.00001
NM_000527.5(LDLR):c.301G>A (p.Glu101Lys)	rs144172724	0.00001
NM_000527.5(LDLR):c.1618G>A (p.Ala540Thr)
NM_000527.5(LDLR):c.1775G>A (p.Gly592Glu)
NM_000527.5(LDLR):c.691T>G (p.Cys231Gly)	rs746091400

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