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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F2
(R314H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely pathogenic
F2
(K345del)
Microsatellite
(inframe_deletion)
Prolonged prothrombin time
GLikely pathogenic
F2
(H605fs)
Deletion
(frameshift variant)
Prolonged prothrombin time
+3 more
GConflicting classifications of pathogenicity
F2
(L609P)
Single nucleotide variant
(missense variant)
Prolonged prothrombin time
GLikely pathogenic
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