"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "XRCC2"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 825672	NM_005431.2(XRCC2):c.534G>A (p.Gln178=)	XRCC2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 137932	NM_005431.2(XRCC2):c.477C>T (p.Arg159=)	XRCC2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 425429	NM_005431.2(XRCC2):c.425C>T (p.Ser142Phe)	XRCC2 (S142F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 137931	NM_005431.2(XRCC2):c.354G>A (p.Val118=)	XRCC2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 183003	NM_005431.2(XRCC2):c.96del (p.Phe32fs)	XRCC2 (F32fs)	Deletion (frameshift variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2583057	GRCh37/hg19 7q34-36.1(chr7:140154317-152551638)x1	KRBA1, LLCFC1 +125 more	Copy number loss	not provided	GPathogenic

ClinVar