"Baylor Genetics"[submitter] AND "XRCC2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 182994	NM_005431.2(XRCC2):c.271C>T (p.Arg91Trp)	XRCC2 (R91W)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 409962	NM_005431.2(XRCC2):c.97G>C (p.Ala33Pro)	XRCC2 (A33P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 625550	GRCh37/hg19 7q32.1-36.3(chr7:128312450-159119220)	ABCB8, ABCF2 +229 more	Copy number gain	not provided	GPathogenic

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