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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGB
(R44C)
Single nucleotide variant
(missense variant)
not provided
+2 more
GLikely pathogenic
FGB
(E191G +1 more)
Single nucleotide variant
(missense variant)
Familial dysfibrinogenemia
+2 more
GUncertain significance
FGB
(D212Y +2 more)
Single nucleotide variant
(missense variant +1 more)
Familial dysfibrinogenemia
GUncertain significance
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