| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Chromosome Breakage Disorders v0.28 | XRCC2 | Zornitza Stark Marked gene: XRCC2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chromosome Breakage Disorders v0.28 | XRCC2 | Zornitza Stark Gene: xrcc2 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chromosome Breakage Disorders v0.28 | XRCC2 | Zornitza Stark Classified gene: XRCC2 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chromosome Breakage Disorders v0.28 | XRCC2 | Zornitza Stark Gene: xrcc2 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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 |
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