ClinVar Miner

List of variants in gene LDLR reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP
NM_000527.4(LDLR):c.*1168G>A rs17242683
NM_000527.4(LDLR):c.*1216dup rs34113544
NM_000527.4(LDLR):c.*1217C>G rs3180023
NM_000527.4(LDLR):c.*1232_*1234CTA[1] rs398059563
NM_000527.4(LDLR):c.*1262T>C rs2915966
NM_000527.4(LDLR):c.*1268C>T rs2978615
NM_000527.4(LDLR):c.*1292C>T rs556381931
NM_000527.4(LDLR):c.*1332G>A rs10415069
NM_000527.4(LDLR):c.*1336C>G rs72658877
NM_000527.4(LDLR):c.*1340C>A rs186461273
NM_000527.4(LDLR):c.*1354T>C rs7258146
NM_000527.4(LDLR):c.*1376T>C rs55903358
NM_000527.4(LDLR):c.*1419C>A rs55971831
NM_000527.4(LDLR):c.*141G>A rs3826810
NM_000527.4(LDLR):c.*1430C>T rs7254521
NM_000527.4(LDLR):c.*1453A>G rs5742911
NM_000527.4(LDLR):c.*1510T>C rs17249057
NM_000527.4(LDLR):c.*1600G>T rs17249064
NM_000527.4(LDLR):c.*1743C>T rs2738467
NM_000527.4(LDLR):c.*2016G>A rs72658879
NM_000527.4(LDLR):c.*2054G>A rs28398082
NM_000527.4(LDLR):c.*2196_*2197TA[7] rs3980933
NM_000527.4(LDLR):c.*315G>C rs2738464
NM_000527.4(LDLR):c.*504G>A rs2738465
NM_000527.4(LDLR):c.*52G>A rs14158
NM_000527.4(LDLR):c.*666T>C rs1433099
NM_000527.4(LDLR):c.*773A>G rs2738466
NM_000527.4(LDLR):c.*982G>C rs10409044
NM_000527.4(LDLR):c.1060+10G>C rs12710260
NM_000527.4(LDLR):c.1060+7= rs2738442
NM_000527.4(LDLR):c.1171G>A (p.Ala391Thr) rs11669576
NM_000527.4(LDLR):c.1413A>G (p.Arg471=) rs5930
NM_000527.4(LDLR):c.1545C>T (p.Asn515=) rs147896205
NM_000527.4(LDLR):c.1617C>T (p.Pro539=) rs5929
NM_000527.4(LDLR):c.1725C>T (p.Leu575=) rs1799898
NM_000527.4(LDLR):c.1773C>T (p.Asn591=) rs688
NM_000527.4(LDLR):c.1959T>C (p.Val653=) rs5925
NM_000527.4(LDLR):c.2232A>G (p.Arg744=) rs5927
NM_000527.4(LDLR):c.81C>T (p.Cys27=) rs2228671
NM_000527.4(LDLR):c.90C>T (p.Asn30=) rs72658855
NM_000527.4(LDLR):c.940+9C>T rs17242906

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