List of variants in gene POLE reported as likely benign for Familial 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006231.4(POLE):c.139C>T (p.Arg47Trp)	rs143626223	0.00082
NM_006231.4(POLE):c.2099C>T (p.Pro700Leu)	rs777002868	0.00002
NM_006231.4(POLE):c.5429A>T (p.His1810Leu)	rs777390504	0.00001

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