RS104886458 FANCC

Health Risk Chr 9:95101723
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What This Variant Does
"[OMIM:?]
Associated Conditions
Fanconi anemia complementation group C
Fanconi anemia
Hereditary cancer-predisposing syndrome
FANCC-related disorder
Fanconi anemia complementation group C
Fanconi anemia
Hereditary cancer-predisposing syndrome
FANCC-related disorder
Other Variants in FANCC
rs121917783 rs104886456 rs121917784 rs104886457 rs794726667 rs104886459 rs121917785 rs794726668 rs587779898 rs377468919
Ask Dr. Hemsworth about this variant