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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F8
(V2242M +1 more)
Single nucleotide variant
(missense variant)
Hereditary factor VIII deficiency disease
GConflicting classifications of pathogenicity
F8
(E1057K)
Single nucleotide variant
(missense variant)
Thrombophilia, X-linked, due to factor 8 defect
+2 more
GConflicting classifications of pathogenicity