RS374854636 VWF

Health Risk Chr 12:6110568
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Associated Conditions
Inborn genetic diseases
von Willebrand disease type 1
Inborn genetic diseases
von Willebrand disease type 1
Other Variants in VWF
rs61750584 rs61750117 rs61750579 rs61749392 rs61749384 rs61749387 rs61749397 rs61749403 rs61748477 rs121964894
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