ClinVar Miner

List of variants in gene CLCN2 reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004366.6(CLCN2):c.1937G>A (p.Arg646Gln)	rs115961753	0.00156
NM_004366.6(CLCN2):c.302T>C (p.Met101Thr)	rs546781274	0.00006

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