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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F5
(H1327R)
Single nucleotide variant
(missense variant)
Congenital factor V deficiency
+4 more
GBenign/Likely benign
F5
(R334T)
Single nucleotide variant
(missense variant)
Thrombophilia due to activated protein C resistance
GPathogenic
F5
(R334G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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