Genomics England
GMS Panels
Panels
Genes and Entities
XRCC1
X-ray repair cross complementing 1
OMIM:
194360
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Panel
Mode of inheritance
Details
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Ataxia and cerebellar anomalies - narrow panel
Component of the following Super Panels:
- Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spinocerebellar ataxia, autosomal recessive 26, OMIM:617633