ClinVar Miner

List of variants in gene POLE reported as uncertain significance for childhood malignant neoplasm

Included ClinVar conditions (10):

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.4169G>A (p.Arg1390His)	rs200776293	0.00011
NM_006231.4(POLE):c.5633G>A (p.Arg1878His)	rs374022997	0.00001

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