ClinVar Miner

List of variants in gene CHEK2 reported as benign for Breast and/or ovarian cancer

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.1343T>G (p.Ile448Ser)	rs17886163	0.00555
NM_007194.4(CHEK2):c.444+19T>C	rs200501745	0.00026

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