ClinVar Miner

List of variants in gene CLCN5 reported as uncertain significance by Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare

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_001127898.4(CLCN5):c.1061C>T (p.Ala354Val)	rs1060499698
NM_001127898.4(CLCN5):c.933+3A>C	rs1602123559

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