List of variants in gene CLCN1 reported as benign by PreventionGenetics, part of Exact Sciences

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000083.3(CLCN1):c.450C>T (p.Tyr150=)	rs56307536	0.00885
NM_000083.3(CLCN1):c.26G>A (p.Arg9His)	rs115379077	0.00775
NM_000083.3(CLCN1):c.663G>A (p.Ala221=)	rs147317366	0.00424
NM_000083.3(CLCN1):c.2509-3C>T	rs375341574	0.00192

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