List of variants in gene CHEK2 reported as likely pathogenic for Breast carcinoma

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.1427C>T (p.Thr476Met)	rs142763740	0.00032
NM_007194.4(CHEK2):c.342G>A (p.Trp114Ter)	rs756949505	0.00001
NM_007194.4(CHEK2):c.660_661del (p.Ile221fs)	rs2146005460
NM_007194.4(CHEK2):c.701_720del (p.Val234fs)	rs2145951528

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