ClinVar Miner

List of variants in gene GLI3 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: 72
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HGVS dbSNP
NM_000168.5(GLI3):c.*3392G>T rs115519476
NM_000168.5(GLI3):c.1029-16dupT rs559579130
NM_000168.5(GLI3):c.827-14dupT rs200073401
NM_000168.6(GLI3):c.*1042dup rs200076691
NM_000168.6(GLI3):c.*1080G>A rs58924064
NM_000168.6(GLI3):c.*1087A>T rs76023240
NM_000168.6(GLI3):c.*11A>G rs139896177
NM_000168.6(GLI3):c.*1297G>A rs116029585
NM_000168.6(GLI3):c.*136T>A rs78794712
NM_000168.6(GLI3):c.*1464A>G rs566417596
NM_000168.6(GLI3):c.*1623A>G rs183853326
NM_000168.6(GLI3):c.*1691C>T rs181261768
NM_000168.6(GLI3):c.*185G>A rs531678760
NM_000168.6(GLI3):c.*2019C>T rs73318085
NM_000168.6(GLI3):c.*2071C>T rs539931592
NM_000168.6(GLI3):c.*2117A>G rs185099021
NM_000168.6(GLI3):c.*2276T>C rs568393106
NM_000168.6(GLI3):c.*2347C>A rs138209843
NM_000168.6(GLI3):c.*2357T>A rs562705224
NM_000168.6(GLI3):c.*249A>T rs6972450
NM_000168.6(GLI3):c.*2620C>G rs56158069
NM_000168.6(GLI3):c.*2715G>A rs193192167
NM_000168.6(GLI3):c.*30G>T rs77886553
NM_000168.6(GLI3):c.*3238C>T rs372628047
NM_000168.6(GLI3):c.*3262A>G rs73096902
NM_000168.6(GLI3):c.*3309C>A rs553151369
NM_000168.6(GLI3):c.*655A>G rs77197280
NM_000168.6(GLI3):c.*726A>G rs118157739
NM_000168.6(GLI3):c.*835G>A rs73688609
NM_000168.6(GLI3):c.*847C>A rs116986447
NM_000168.6(GLI3):c.*943G>A rs139782938
NM_000168.6(GLI3):c.-68G>A rs113629469
NM_000168.6(GLI3):c.1028+15G>A rs116842918
NM_000168.6(GLI3):c.1029-11C>T rs116195563
NM_000168.6(GLI3):c.1393G>C (p.Gly465Arg) rs35488756
NM_000168.6(GLI3):c.1485G>A (p.Glu495=) rs149248727
NM_000168.6(GLI3):c.1497C>T (p.His499=) rs539144173
NM_000168.6(GLI3):c.1509C>T (p.Asn503=) rs34020684
NM_000168.6(GLI3):c.1647+13G>A rs149955824
NM_000168.6(GLI3):c.1843A>T (p.Thr615Ser) rs200913720
NM_000168.6(GLI3):c.1959G>A (p.Pro653=) rs148226583
NM_000168.6(GLI3):c.2083G>A (p.Val695Ile) rs199606102
NM_000168.6(GLI3):c.2179G>A (p.Gly727Arg) rs121917710
NM_000168.6(GLI3):c.2424A>G (p.Ile808Met) rs62622373
NM_000168.6(GLI3):c.2635G>A (p.Ala879Thr) rs137939155
NM_000168.6(GLI3):c.280C>T (p.Leu94=) rs115137047
NM_000168.6(GLI3):c.2826G>C (p.Pro942=) rs34245321
NM_000168.6(GLI3):c.2835G>C (p.Leu945=) rs61758978
NM_000168.6(GLI3):c.3015C>T (p.Ala1005=) rs200965852
NM_000168.6(GLI3):c.3083G>T (p.Ser1028Ile) rs79049330
NM_000168.6(GLI3):c.3084C>T (p.Ser1028=) rs79703713
NM_000168.6(GLI3):c.3117G>A (p.Ala1039=) rs75796620
NM_000168.6(GLI3):c.3208A>T (p.Thr1070Ser) rs150907867
NM_000168.6(GLI3):c.341G>A (p.Arg114Lys) rs146458902
NM_000168.6(GLI3):c.3598C>G (p.His1200Asp) rs145069572
NM_000168.6(GLI3):c.3664C>T (p.Pro1222Ser) rs118149040
NM_000168.6(GLI3):c.3762T>C (p.Tyr1254=) rs148043302
NM_000168.6(GLI3):c.3774C>G (p.Leu1258=) rs35448119
NM_000168.6(GLI3):c.3894G>A (p.Pro1298=) rs530418832
NM_000168.6(GLI3):c.3935T>G (p.Met1312Arg) rs199875457
NM_000168.6(GLI3):c.3984C>T (p.Leu1328=) rs148940743
NM_000168.6(GLI3):c.4005G>A (p.Pro1335=) rs149860242
NM_000168.6(GLI3):c.4007G>A (p.Gly1336Glu) rs35280470
NM_000168.6(GLI3):c.4020C>T (p.Pro1340=) rs35139358
NM_000168.6(GLI3):c.444C>T (p.Tyr148=) rs142241970
NM_000168.6(GLI3):c.4510A>C (p.Ile1504Leu) rs145419251
NM_000168.6(GLI3):c.4524C>T (p.Ala1508=) rs201112421
NM_000168.6(GLI3):c.4533C>T (p.Asp1511=) rs145513625
NM_000168.6(GLI3):c.4609C>T (p.Arg1537Cys) rs35364414
NM_000168.6(GLI3):c.474-4C>T rs74536326
NM_000168.6(GLI3):c.501G>A (p.Thr167=) rs149901929
NM_000168.6(GLI3):c.840C>G (p.Ser280=) rs77084911

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