ClinVar Miner

List of variants in gene GLI2 reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001374353.1(GLI2):c.1183-12C>T	rs2467712063	0.00001
NM_001374353.1(GLI2):c.3452A>G (p.Gln1151Arg)	rs2467778263

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