List of variants in gene CLCN1 reported as benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_000083.3(CLCN1):c.352G>T (p.Gly118Trp)	rs10282312	0.98349
NM_000083.3(CLCN1):c.1402-9C>T	rs2272252	0.43982
NM_000083.3(CLCN1):c.2180C>T (p.Pro727Leu)	rs13438232	0.39795

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