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

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.1100del (p.Thr367fs)	rs555607708	0.00181
NM_007194.4(CHEK2):c.444+1G>A	rs121908698	0.00009
NM_007194.4(CHEK2):c.499G>A (p.Gly167Arg)	rs72552322	0.00001
NM_007194.4(CHEK2):c.58C>T (p.Gln20Ter)	rs536907995
NM_007194.4(CHEK2):c.847-1G>A	rs878854926

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