ClinVar Miner

List of variants in gene XRCC2 reported as benign for Hereditary cancer-predisposing syndrome

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005431.2(XRCC2):c.*1T>C	rs3218539	0.04983
NM_005431.2(XRCC2):c.563G>A (p.Arg188His)	rs3218536	0.04933

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