List of variants in gene PCSK9 reported as benign by Laboratorium voor Moleculaire Diagnostiek Experimentele Vasculaire Geneeskunde, Academisch Medisch Centrum

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_174936.4(PCSK9):c.1026A>G (p.Gln342=)	rs509504	0.98223
NM_174936.4(PCSK9):c.1380A>G (p.Val460=)	rs540796	0.82761
NM_174936.4(PCSK9):c.799+3A>G	rs2495477	0.49156
NM_174936.4(PCSK9):c.658-7C>T	rs2483205	0.45035
NM_174936.4(PCSK9):c.207+209C>T	rs11583723	0.09478
NM_174936.4(PCSK9):c.657+9G>A	rs11800243	0.03991
NM_174936.4(PCSK9):c.1119C>T (p.Ser373=)	rs139683719	0.00002
NM_174936.4(PCSK9):c.-168C>A	rs1553135350
NM_174936.4(PCSK9):c.1420G>A (p.Val474Ile)
NM_174936.4(PCSK9):c.158C>T (p.Ala53Val)
NM_174936.4(PCSK9):c.2009G>A (p.Gly670Glu)
NM_174936.4(PCSK9):c.250G>A (p.Glu84Lys)	rs1553135931
NM_174936.4(PCSK9):c.45GCT[6] (p.Leu23del)
NM_174936.4(PCSK9):c.45GCT[8] (p.Leu23dup)	rs35574083
NM_174936.4(PCSK9):c.45GCT[9] (p.Leu22_Leu23dup)	rs35574083

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