List of variants in gene CLCN2 reported as benign for idiopathic generalized epilepsy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004366.6(CLCN2):c.2063G>A (p.Arg688Gln)	rs111656822	0.01603
NM_004366.6(CLCN2):c.2271+8T>G	rs114350071	0.01055
NM_004366.6(CLCN2):c.2415+9A>G	rs192449317	0.00351

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