ClinVar Miner

List of variants in gene combination LOC130009266, POLE reported as uncertain significance 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_006231.4(POLE):c.44C>T (p.Ala15Val)	rs1565986587	0.00001
NM_006231.4(POLE):c.1A>T (p.Met1Leu)	rs878854847

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