List of variants in gene CLCN2 reported as likely pathogenic for Epilepsy, idiopathic generalized, susceptibility to, 11; Familial hyperaldosteronism type II; Leukoencephalopathy with mild cerebellar ataxia and white matter edema

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_004366.6(CLCN2):c.898+1G>A	rs141074059	0.00009
NM_004366.6(CLCN2):c.1709G>A (p.Trp570Ter)	rs201330912	0.00002
NM_004366.6(CLCN2):c.925C>T (p.Arg309Ter)	rs863225250	0.00001
NM_004366.6(CLCN2):c.1069del (p.Arg357fs)
NM_004366.6(CLCN2):c.1828C>T (p.Arg610Ter)
NM_004366.6(CLCN2):c.194del (p.Gly65fs)
NM_004366.6(CLCN2):c.221-2A>G
NM_004366.6(CLCN2):c.64-1G>A
NM_004366.6(CLCN2):c.668_672del (p.Leu223fs)	rs756385625

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