Variants in gene XRCC2 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 11

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HGVS	dbSNP	gnomAD frequency
NM_005431.2(XRCC2):c.808T>G (p.Phe270Val)	rs145085742	0.00205
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.39+8C>G	rs200363289	0.00006
NM_005431.2(XRCC2):c.390T>G (p.Leu130=)	rs752735963	0.00001
NM_005431.2(XRCC2):c.121+3dup	rs1064794394
NM_005431.2(XRCC2):c.726C>T (p.Ser242=)	rs2116987114
NM_005431.2(XRCC2):c.825T>C (p.Ser275=)	rs770438650

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