ClinVar Miner

List of variants in gene GLI3 reported as benign by GeneDx

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Gene type:
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Total variants: 24
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HGVS dbSNP
NC_000007.13:g.42007664del
NC_000007.14:g.42223444del
NM_000168.6(GLI3):c.1028+281G>T
NM_000168.6(GLI3):c.1029-11C>T rs116195563
NM_000168.6(GLI3):c.1029-22dup rs559579130
NM_000168.6(GLI3):c.1029-7C>T rs78280303
NM_000168.6(GLI3):c.125-263A>G
NM_000168.6(GLI3):c.1356+64C>A
NM_000168.6(GLI3):c.1393G>C (p.Gly465Arg) rs35488756
NM_000168.6(GLI3):c.1497+256C>T
NM_000168.6(GLI3):c.1647+13G>A rs149955824
NM_000168.6(GLI3):c.1647+226C>A
NM_000168.6(GLI3):c.2431+123G>A
NM_000168.6(GLI3):c.280C>T (p.Leu94=) rs115137047
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.3208A>T (p.Thr1070Ser) rs150907867
NM_000168.6(GLI3):c.341G>A (p.Arg114Lys) rs146458902
NM_000168.6(GLI3):c.3664C>T (p.Pro1222Ser) rs118149040
NM_000168.6(GLI3):c.368-19G>A rs79879393
NM_000168.6(GLI3):c.368-248C>T
NM_000168.6(GLI3):c.826+255T>C
NM_000168.6(GLI3):c.827-181C>T

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