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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F8
(R1708C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
F8
(T154I)
Single nucleotide variant
(missense variant)
Hereditary factor VIII deficiency disease
GUncertain significance