Variants in gene PCSK9 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
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	gnomAD frequency
NM_174936.4(PCSK9):c.1069C>T (p.Arg357Cys)	rs148562777	0.00012
NM_174936.4(PCSK9):c.103G>T (p.Asp35Tyr)	rs764603059	0.00001
NM_174936.4(PCSK9):c.1486C>T (p.Arg496Trp)	rs374603772	0.00001
NM_174936.4(PCSK9):c.1120G>T (p.Asp374Tyr)	rs137852912
NM_174936.4(PCSK9):c.1394C>T (p.Ser465Leu)	rs778849441
NM_174936.4(PCSK9):c.1496G>A (p.Arg499His)	rs143394031
NM_174936.4(PCSK9):c.381T>A (p.Ser127Arg)	rs28942111
NM_174936.4(PCSK9):c.385G>A (p.Asp129Asn)
NM_174936.4(PCSK9):c.386A>G (p.Asp129Gly)	rs1553135971
NM_174936.4(PCSK9):c.644G>A (p.Arg215His)	rs794728683
NM_174936.4(PCSK9):c.94G>A (p.Glu32Lys)

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