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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGA
(L636fs)
Duplication
(frameshift variant)
See cases
GLikely pathogenic
FGA
(G350R)
Single nucleotide variant
(missense variant)
Stroke disorder
+1 more
GUncertain significance
FGA
(V159I)
Single nucleotide variant
(missense variant)
Stroke disorder
GUncertain significance
FGA
(V40fs)
Deletion
(frameshift variant)
Familial dysfibrinogenemia
+1 more
GPathogenic/Likely pathogenic
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