ClinVar Miner

List of variants in gene CSNK2B reported as likely pathogenic for CSNK2B-related disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001320.7(CSNK2B):c.175+1G>A	rs2536958403
NM_001320.7(CSNK2B):c.558-2A>C
NM_001320.7(CSNK2B):c.94G>A (p.Asp32Asn)	rs1554169984

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