List of variants in gene GLI3 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000168.6(GLI3):c.4510A>C (p.Ile1504Leu)	rs145419251	0.00424
NM_000168.6(GLI3):c.341G>A (p.Arg114Lys)	rs146458902	0.00274
NM_000168.6(GLI3):c.840C>G (p.Ser280=)	rs77084911	0.00198
NM_000168.6(GLI3):c.2424A>G (p.Ile808Met)	rs62622373	0.00194
NM_000168.6(GLI3):c.*2666G>A	rs117987369	0.00142
NM_000168.6(GLI3):c.3935T>G (p.Met1312Arg)	rs199875457	0.00027
NM_000168.6(GLI3):c.3598C>G (p.His1200Asp)	rs145069572	0.00025
NM_000168.6(GLI3):c.363C>T (p.His121=)	rs150295615	0.00008
NM_000168.6(GLI3):c.*248dup	rs5883809
NM_000168.6(GLI3):c.*2859G>A

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