RS397509404 ERCC4

Health Risk Chr 16:13935661
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What This Variant Does
"CLNSIG=5
Associated Conditions
Xeroderma pigmentosum
type F/Cockayne syndrome
Spastic ataxia
Cockayne syndrome
group F
Fanconi anemia complementation group Q
Xeroderma pigmentosum
type F/Cockayne syndrome
Spastic ataxia
Cockayne syndrome
group F
Fanconi anemia complementation group Q
Other Variants in ERCC4
rs869025184 rs121913049 rs121913050 rs397509400 rs149364215 rs397509401 rs397509402 rs397509403 rs147105770 rs374186605
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