RS772432152 ERCC4

Health Risk Chr 16:13930832
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What This Variant Does
"CLNSIG=4
Associated Conditions
Xeroderma pigmentosum
group F
Fanconi anemia complementation group Q
Cockayne syndrome
XFE progeroid syndrome
Xeroderma pigmentosum
group F
Fanconi anemia complementation group Q
Cockayne syndrome
XFE progeroid syndrome
Other Variants in ERCC4
rs869025184 rs121913049 rs121913050 rs397509400 rs149364215 rs397509401 rs397509402 rs397509403 rs397509404 rs147105770
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