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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGB
(R47*)
Single nucleotide variant
(nonsense)
Hypofibrinogenemia
GLikely pathogenic
FGB
(P265L +1 more)
Single nucleotide variant
(missense variant)
Thrombus
+7 more
GConflicting classifications of pathogenicity