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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F9
(R75*)
Single nucleotide variant
(nonsense)
Hereditary factor IX deficiency disease
GPathogenic
F9
(R346L)
Single nucleotide variant
(missense variant)
Thrombophilia, X-linked, due to factor 9 defect
GPathogenic