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

Minimum submission review status:		Collection method:
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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP
NM_000168.6(GLI3):c.*11A>G	rs139896177
NM_000168.6(GLI3):c.*15dup	rs886038264
NM_000168.6(GLI3):c.1029-22dup	rs559579130
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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