List of variants in gene CLCN2 reported as likely pathogenic for adrenal gland neoplasm

Minimum submission review status:		Collection method:
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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004366.6(CLCN2):c.898+1G>A	rs141074059	0.00009
NM_004366.6(CLCN2):c.1412G>A (p.Arg471His)	rs771507094	0.00004
NM_004366.6(CLCN2):c.1709G>A (p.Trp570Ter)	rs201330912	0.00002
NM_004366.6(CLCN2):c.668_672del (p.Leu223fs)	rs756385625

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