List of variants in gene CHEK2 reported as likely 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.254C>T (p.Pro85Leu)	rs17883862	0.00201
NM_007194.4(CHEK2):c.1407G>A (p.Val469=)	rs17881378	0.00190
NM_007194.4(CHEK2):c.410G>A (p.Arg137Gln)	rs368570187	0.00012
NM_007194.4(CHEK2):c.1217G>A (p.Arg406His)	rs200649225	0.00009
NM_007194.4(CHEK2):c.1260-10C>G	rs730881706	0.00006
NM_007194.4(CHEK2):c.542G>A (p.Arg181His)	rs121908701	0.00006
NM_007194.4(CHEK2):c.1336A>G (p.Asn446Asp)	rs121908705	0.00004
NM_007194.4(CHEK2):c.15G>A (p.Ser5=)	rs145183886	0.00004
NM_007194.4(CHEK2):c.528G>C (p.Gly176=)	rs587780889	0.00001
NM_007194.4(CHEK2):c.612G>T (p.Leu204=)	rs752876192
NM_007194.4(CHEK2):c.981T>C (p.Tyr327=)	rs1601738446

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