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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F5
(N741S)
Single nucleotide variant
(missense variant)
Congenital factor V deficiency
+6 more
GConflicting classifications of pathogenicity
F2
(G267W)
Single nucleotide variant
(missense variant)
Thrombophilia due to thrombin defect
GUncertain significance