ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_000168.5(GLI3):c.1029-16dupT rs559579130
NM_000168.6(GLI3):c.*11A>G rs139896177
NM_000168.6(GLI3):c.*15dup rs886038264
NM_000168.6(GLI3):c.1242+25C>T rs375904354
NM_000168.6(GLI3):c.1242+42C>G rs772766325
NM_000168.6(GLI3):c.1243-40A>C rs77659679
NM_000168.6(GLI3):c.1357-17C>G rs190600888
NM_000168.6(GLI3):c.1813-47G>A rs199956247
NM_000168.6(GLI3):c.1911T>C (p.His637=) rs886038265
NM_000168.6(GLI3):c.2104-50C>T rs115463742
NM_000168.6(GLI3):c.2184C>T (p.Leu728=) rs149724824
NM_000168.6(GLI3):c.2373G>A (p.Pro791=) rs61754622
NM_000168.6(GLI3):c.2432-30C>T rs374365217
NM_000168.6(GLI3):c.3001G>A (p.Gly1001Ser) rs202182779
NM_000168.6(GLI3):c.3312C>T (p.Asn1104=) rs770842648
NM_000168.6(GLI3):c.3540G>A (p.Gly1180=) rs143551701
NM_000168.6(GLI3):c.3772C>G (p.Leu1258Val) rs754908186
NM_000168.6(GLI3):c.3894G>A (p.Pro1298=) rs530418832
NM_000168.6(GLI3):c.528C>G (p.Ile176Met) rs539622820
NM_000168.6(GLI3):c.679+40C>A rs367979286
NM_000168.6(GLI3):c.680-25C>T rs55872291
NM_000168.6(GLI3):c.743G>A (p.Arg248His) rs186337909
NM_000168.6(GLI3):c.840C>G (p.Ser280=) rs77084911

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