ClinVar Miner

List of variants in gene CSNK2B reported as not provided

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_001320.7(CSNK2B):c.367+5del	rs1583610622
NM_001320.7(CSNK2B):c.70G>T (p.Glu24Ter)	rs2151182211

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