List of variants in gene GLI3 reported as benign by Eurofins NTD LLC (GA)

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: 12

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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.4071C>T (p.Tyr1357=)	rs34089404	0.07043
NM_000168.6(GLI3):c.2835G>C (p.Leu945=)	rs61758978	0.01858
NM_000168.6(GLI3):c.2179G>A (p.Gly727Arg)	rs121917710	0.00511
NM_000168.6(GLI3):c.1393G>C (p.Gly465Arg)	rs35488756	0.00320
NM_000168.6(GLI3):c.2373G>A (p.Pro791=)	rs61754622	0.00267
NM_000168.6(GLI3):c.1357-17C>G	rs190600888	0.00256
NM_000168.6(GLI3):c.2424A>G (p.Ile808Met)	rs62622373	0.00194
NM_000168.6(GLI3):c.2826G>C (p.Pro942=)	rs34245321
NM_000168.6(GLI3):c.3083_3084delinsTT (p.Ser1028Ile)	rs886043721

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