List of variants in gene CSNK2B reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001320.7(CSNK2B):c.582G>A (p.Pro194=)	rs547417484	0.00007
NM_001320.7(CSNK2B):c.468C>T (p.Gly156=)
NM_001320.7(CSNK2B):c.516C>T (p.Pro172=)

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