RS121917786 FANCD2

Health Risk Chr 3:10090315
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What This Variant Does
"[OMIM:?]
Associated Conditions
Fanconi anemia complementation group D2
Inborn genetic diseases
Fanconi anemia
Fanconi anemia complementation group D2
Inborn genetic diseases
Fanconi anemia
Other Variants in FANCD2
rs121917787 rs121917788 rs147523071 rs587778331 rs200971205 rs369823368 rs4019784 rs143936557 rs116736407 rs375412395
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