RS191943709 FANCA

Health Risk Chr 16:89758617
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Fanconi anemia
Fanconi anemia complementation group A
Inborn genetic diseases
Fanconi anemia
Fanconi anemia complementation group A
Other Variants in FANCA
rs397507552 rs778507965 rs747851434 rs587776570 rs121907930 rs794726660 rs13336566 rs148100796 rs199967286 rs587778312
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