List of variants in gene POLE reported as likely pathogenic by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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_006231.4(POLE):c.2731del (p.Gln911fs)	rs1555226051
NM_006231.4(POLE):c.3264_3275+13del	rs761516512
NM_006231.4(POLE):c.3378+3G>T
NM_006231.4(POLE):c.5156C>A (p.Ser1719Ter)

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