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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F8
(M2257V +1 more)
Single nucleotide variant
(missense variant)
Hereditary factor VIII deficiency disease
GBenign
F8
(D1260E)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign