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| Chromosome Breakage Disorders v0.14 | RFWD3 | Zornitza Stark Marked gene: RFWD3 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chromosome Breakage Disorders v0.14 | RFWD3 | Zornitza Stark Gene: rfwd3 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chromosome Breakage Disorders v0.14 | RFWD3 |
Zornitza Stark gene: RFWD3 was added gene: RFWD3 was added to Chromosome Breakage Disorders. Sources: Expert list Mode of inheritance for gene: RFWD3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: RFWD3 were set to 28691929 Phenotypes for gene: RFWD3 were set to Fanconi anemia, complementation group W, MIM# 617784 Review for gene: RFWD3 was set to RED Added comment: Single family reported, functional data. Sources: Expert list |
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