List of variants in gene GLI2 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001374353.1(GLI2):c.3539G>A (p.Gly1180Asp)	rs114823319	0.00522
NM_001374353.1(GLI2):c.803C>T (p.Ala268Val)	rs146992756	0.00254
NM_001374353.1(GLI2):c.3298G>T (p.Val1100Leu)	rs147580961	0.00222
NM_001374353.1(GLI2):c.2437T>C (p.Phe813Leu)	rs556743028	0.00106

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