List of variants in gene GLI3 reported as benign by PreventionGenetics, part of Exact Sciences

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

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_000168.6(GLI3):c.1356+11G>C	rs846273	0.97240
NM_000168.6(GLI3):c.547A>G (p.Thr183Ala)	rs846266	0.64495
NM_000168.6(GLI3):c.2993C>T (p.Pro998Leu)	rs929387	0.31467
NM_000168.6(GLI3):c.1498-44G>A	rs17707162	0.08936
NM_000168.6(GLI3):c.900C>T (p.Ser300=)	rs35961850	0.07677
NM_000168.6(GLI3):c.537C>T (p.His179=)	rs3898405	0.07173
NM_000168.6(GLI3):c.4071C>T (p.Tyr1357=)	rs34089404	0.07043
NM_000168.6(GLI3):c.*30G>T	rs77886553	0.03497
NM_000168.6(GLI3):c.4609C>T (p.Arg1537Cys)	rs35364414	0.03460
NM_000168.6(GLI3):c.4007G>A (p.Gly1336Glu)	rs35280470	0.03456
NM_000168.6(GLI3):c.2835G>C (p.Leu945=)	rs61758978	0.01858
NM_000168.6(GLI3):c.3774C>G (p.Leu1258=)	rs35448119	0.01377
NM_000168.6(GLI3):c.3083G>T (p.Ser1028Ile)	rs79049330	0.01304
NM_000168.6(GLI3):c.3084C>T (p.Ser1028=)	rs79703713	0.01303
NM_000168.6(GLI3):c.1029-7C>T	rs78280303	0.01279
NM_000168.6(GLI3):c.1029-11C>T	rs116195563	0.00867
NM_000168.6(GLI3):c.368-19G>A	rs79879393	0.00858
NM_000168.6(GLI3):c.2802G>A (p.Ala934=)	rs61730503	0.00520
NM_000168.6(GLI3):c.2165A>G (p.Asn722Ser)	rs146130351	0.00514
NM_000168.6(GLI3):c.1393G>C (p.Gly465Arg)	rs35488756	0.00320
NM_000168.6(GLI3):c.840C>G (p.Ser280=)	rs77084911	0.00198
NM_000168.6(GLI3):c.3015C>T (p.Ala1005=)	rs200965852	0.00032
NM_000168.6(GLI3):c.3117G>A (p.Ala1039=)	rs75796620	0.00019
NM_000168.6(GLI3):c.3894G>A (p.Pro1298=)	rs530418832	0.00006
NM_000168.6(GLI3):c.1509C>T (p.Asn503=)	rs34020684
NM_000168.6(GLI3):c.2826G>C (p.Pro942=)	rs34245321
NM_000168.6(GLI3):c.4020C>T (p.Pro1340=)	rs35139358

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