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Date	Panel	Item	Activity
Filter activities 6 actions
14 Apr 2026	Chromosome Breakage Disorders v2.0	XRCC2	Gene migrated from ENSG00000196584 to ENSG00000196584 (gene set migration)
15 Sep 2020	Chromosome Breakage Disorders v0.28	XRCC2	Zornitza Stark Marked gene: XRCC2 as ready
15 Sep 2020	Chromosome Breakage Disorders v0.28	XRCC2	Zornitza Stark Gene: xrcc2 has been classified as Amber List (Moderate Evidence).
15 Sep 2020	Chromosome Breakage Disorders v0.28	XRCC2	Zornitza Stark Classified gene: XRCC2 as Amber List (moderate evidence)
15 Sep 2020	Chromosome Breakage Disorders v0.28	XRCC2	Zornitza Stark Gene: xrcc2 has been classified as Amber List (Moderate Evidence).
15 Sep 2020	Chromosome Breakage Disorders v0.27	XRCC2	Zornitza Stark gene: XRCC2 was added gene: XRCC2 was added to Chromosome Breakage Disorders. Sources: Expert list Mode of inheritance for gene: XRCC2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: XRCC2 were set to 27208205; 22232082; 11118202 Phenotypes for gene: XRCC2 were set to Fanconi anemia, complementation group U, MIM# 617247 Review for gene: XRCC2 was set to AMBER Added comment: Single family reported, functional data. Sources: Expert list