ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP
NM_000208.3(INSR):c.*4794T>C rs10415841
NM_000208.3(INSR):c.*4802C>T rs12150997
NM_000208.4(INSR):c.*104A>G rs1051690
NM_000208.4(INSR):c.*1416del rs3833238
NM_000208.4(INSR):c.*1494G>A rs3745550
NM_000208.4(INSR):c.*1974_*1975del rs148930499
NM_000208.4(INSR):c.*2010G>A rs55972112
NM_000208.4(INSR):c.*2779G>A rs3745551
NM_000208.4(INSR):c.*2793C>A rs9282760
NM_000208.4(INSR):c.*2854G>T rs1864193
NM_000208.4(INSR):c.*288del rs35434645
NM_000208.4(INSR):c.*3592A>G rs75499056
NM_000208.4(INSR):c.*3623A>G rs77859571
NM_000208.4(INSR):c.*3857C>T rs114405975
NM_000208.4(INSR):c.*4186T>C rs1366600
NM_000208.4(INSR):c.*4195T>C rs1366601
NM_000208.4(INSR):c.*4218G>C rs10416396
NM_000208.4(INSR):c.*4270G>A rs74433419
NM_000208.4(INSR):c.*4422G>T rs12642
NM_000208.4(INSR):c.*4474C>T rs1052371
NM_000208.4(INSR):c.*784C>G rs1051651
NM_000208.4(INSR):c.*930dup rs34045095
NM_000208.4(INSR):c.1638C>T (p.Asp546=) rs2229429
NM_000208.4(INSR):c.1650G>A (p.Ala550=) rs2059806
NM_000208.4(INSR):c.1862-4A>G rs2245649
NM_000208.4(INSR):c.1918C>T (p.Leu640=) rs2963
NM_000208.4(INSR):c.1932A>C (p.Pro644=) rs2245655
NM_000208.4(INSR):c.2007C>T (p.Phe669=) rs2962
NM_000208.4(INSR):c.2595C>T (p.Asn865=) rs2229431
NM_000208.4(INSR):c.3033C>T (p.Tyr1011=) rs1799815
NM_000208.4(INSR):c.3255C>T (p.His1085=) rs1799817
NM_000208.4(INSR):c.3795-5C>T rs78312382
NM_000208.4(INSR):c.5C>G (p.Ala2Gly) rs7508518
NM_000208.4(INSR):c.653-23TC[11] rs3835070
NM_000208.4(INSR):c.783C>T (p.Asp261=) rs891087

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