RS137852428 F8
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hereditary factor VIII deficiency disease
Hereditary factor IX deficiency disease
Thrombophilia
X-linked
due to factor 8 defect
Familial aortopathy
Hereditary factor VIII deficiency disease
Hereditary factor IX deficiency disease
Thrombophilia
X-linked
due to factor 8 defect
Familial aortopathy
Other Variants in F8