RS1800069 ERCC4

Health Risk Chr 16:13947713
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Associated Conditions
Xeroderma pigmentosum
group F
Cockayne syndrome
Fanconi anemia complementation group Q
XFE progeroid syndrome
Inborn genetic diseases
ERCC4-related disorder
Hereditary cancer-predisposing syndrome
Xeroderma pigmentosum
group F
Cockayne syndrome
Fanconi anemia complementation group Q
XFE progeroid syndrome
Inborn genetic diseases
ERCC4-related disorder
Other Variants in ERCC4
rs869025184 rs121913049 rs121913050 rs397509400 rs149364215 rs397509401 rs397509402 rs397509403 rs397509404 rs147105770
Ask Dr. Hemsworth about this variant