List of variants in gene LDLR reported as likely benign by Quest Diagnostics Nichols Institute San Juan Capistrano

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000527.4(LDLR):c.-217C>T	rs17249141	0.00338
NM_000527.5(LDLR):c.67+18C>A	rs17242759	0.00319
NM_000527.5(LDLR):c.2055G>A (p.Pro685=)	rs149126953	0.00040
NM_000527.5(LDLR):c.564C>T (p.Tyr188=)	rs121908034	0.00016
NM_000527.5(LDLR):c.165C>G (p.Gly55=)	rs150644181	0.00015
NM_000527.5(LDLR):c.1431C>T (p.Asp477=)	rs368610522	0.00003
NM_000527.5(LDLR):c.1104C>T (p.Cys368=)	rs113669610	0.00002
NM_000527.5(LDLR):c.2064C>T (p.Asn688=)	rs142279332	0.00002
NM_000527.5(LDLR):c.1635G>A (p.Gly545=)	rs767602284	0.00001
NM_000527.5(LDLR):c.148G>T (p.Ala50Ser)	rs137853960
NM_000527.5(LDLR):c.2073G>A (p.Ser691=)	rs146869252
NM_000527.5(LDLR):c.2289G>T (p.Glu763Asp)	rs774698247
NM_000527.5(LDLR):c.270T>C (p.Asp90=)	rs372828849
NM_000527.5(LDLR):c.829G>A (p.Glu277Lys)

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