List of variants in gene XRCC2 reported as benign for not specified

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_005431.2(XRCC2):c.*1T>C	rs3218539	0.04983
NM_005431.2(XRCC2):c.40-10C>T	rs3218472	0.01055
NM_005431.2(XRCC2):c.-50G>A	rs139350845	0.00175
NM_005431.2(XRCC2):c.40-16T>C	rs41274991	0.00141
NM_005431.2(XRCC2):c.354G>A (p.Val118=)	rs558977371	0.00012
NM_005431.2(XRCC2):c.678T>C (p.Tyr226=)	rs143357617	0.00010
NM_005431.2(XRCC2):c.477C>T (p.Arg159=)	rs202226401	0.00008
NM_005431.2(XRCC2):c.282A>G (p.Thr94=)	rs376598559	0.00006
NM_005431.2(XRCC2):c.-48G>A	rs372428897	0.00002
NM_005431.2(XRCC2):c.300A>G (p.Leu100=)	rs146700851	0.00001

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