ClinVar Miner

List of variants in gene GLI3 reported as likely benign by GeneDx

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Gene type:
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Total variants: 23
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HGVS dbSNP
NM_000168.6(GLI3):c.124+10A>G rs112576935
NM_000168.6(GLI3):c.1242+16C>T rs754808194
NM_000168.6(GLI3):c.1287G>A (p.Pro429=) rs760816574
NM_000168.6(GLI3):c.1357-17C>G rs190600888
NM_000168.6(GLI3):c.2006C>T (p.Thr669Ile) rs139108417
NM_000168.6(GLI3):c.2104-8C>T rs769769944
NM_000168.6(GLI3):c.211G>A (p.Val71Ile) rs143843875
NM_000168.6(GLI3):c.2179G>A (p.Gly727Arg) rs121917710
NM_000168.6(GLI3):c.2245A>G (p.Ile749Val) rs140048578
NM_000168.6(GLI3):c.2373G>A (p.Pro791=) rs61754622
NM_000168.6(GLI3):c.2424A>G (p.Ile808Met) rs62622373
NM_000168.6(GLI3):c.3453C>T (p.Pro1151=) rs749508811
NM_000168.6(GLI3):c.3598C>G (p.His1200Asp) rs145069572
NM_000168.6(GLI3):c.3829C>G (p.Gln1277Glu) rs146582871
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.411T>C (p.Ile137=) rs200203051
NM_000168.6(GLI3):c.444C>T (p.Tyr148=) rs142241970
NM_000168.6(GLI3):c.474-4C>T rs74536326
NM_000168.6(GLI3):c.501G>A (p.Thr167=) rs149901929
NM_000168.6(GLI3):c.563C>A (p.Ser188Tyr) rs369926331
NM_000168.6(GLI3):c.680-10C>T rs1035936832
NM_000168.6(GLI3):c.680-14_680-13del

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