RS149364215 ERCC4

Health Risk Chr 16:13947661
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What This Variant Does
"CLNSIG=5
Associated Conditions
Fanconi anemia complementation group Q
Cockayne syndrome
Xeroderma pigmentosum
group F
XFE progeroid syndrome
ERCC4-Related Disorders
Fanconi anemia complementation group Q
Cockayne syndrome
Xeroderma pigmentosum
group F
XFE progeroid syndrome
ERCC4-Related Disorders
Other Variants in ERCC4
rs869025184 rs121913049 rs121913050 rs397509400 rs397509401 rs397509402 rs397509403 rs397509404 rs147105770 rs374186605
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