List of variants in gene CSNK2A1 reported as likely pathogenic by GenomeConnect - Simons Searchlight

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_177559.3(CSNK2A1):c.239G>A (p.Arg80His)	rs1057518092
NM_177559.3(CSNK2A1):c.466G>T (p.Asp156Tyr)	rs1568512728
NM_177559.3(CSNK2A1):c.468T>A (p.Asp156Glu)	rs1064795110

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