ClinVar Miner

List of variants in gene combination CLCNKB, LOC106501713 reported as pathogenic by Genomic Research Center, Shahid Beheshti University of Medical 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000085.5(CLCNKB):c.656-31del	rs751608665	0.00046
NM_000085.5(CLCNKB):c.1476del (p.Gly493fs)	rs1159737562

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