List of variants in gene CLCN2 studied for Familial hyperaldosteronism type II

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_004366.6(CLCN2):c.1934G>A (p.Arg645Gln)	rs375401465	0.00007
NM_004366.6(CLCN2):c.1412G>A (p.Arg471His)	rs771507094	0.00004
NM_004366.6(CLCN2):c.515G>A (p.Arg172Gln)	rs1293789661	0.00001
NM_004366.6(CLCN2):c.1084A>T (p.Lys362Ter)	rs1553856214
NM_004366.6(CLCN2):c.1856-6G>A
NM_004366.6(CLCN2):c.1912G>A (p.Ala638Thr)
NM_004366.6(CLCN2):c.2593A>C (p.Ser865Arg)	rs1553853557
NM_004366.6(CLCN2):c.482G>C (p.Gly161Ala)
NM_004366.6(CLCN2):c.65T>A (p.Met22Lys)	rs758379595
NM_004366.6(CLCN2):c.71G>A (p.Gly24Asp)	rs1085307938
NM_004366.6(CLCN2):c.76T>A (p.Tyr26Asn)	rs1553857113

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