List of variants in gene CHEK2 reported as not provided for colorectal 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.1525C>T (p.Pro509Ser)	rs587780179	0.00014
NM_007194.4(CHEK2):c.1265G>A (p.Ser422Asn)	rs549755590	0.00001

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