RS147105770 ERCC4
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What This Variant Does
"CLNSIG=5
Associated Conditions
Xeroderma pigmentosum
type F/Cockayne syndrome
Fanconi anemia complementation group Q
group F
Cockayne syndrome
XFE progeroid syndrome
ERCC4-related disorder
Autosomal recessive cerebellar ataxia
Xeroderma pigmentosum
type F/Cockayne syndrome
Fanconi anemia complementation group Q
group F
Cockayne syndrome
XFE progeroid syndrome
ERCC4-related disorder
Other Variants in ERCC4