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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F13B
(H532Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
F13B
(R315C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
F13B
Single nucleotide variant
(intron variant)
not specified
+1 more
GUncertain significance
F13B
(Y100*)
Insertion
(nonsense)
Coagulation factor deficiency syndrome
+1 more
GPathogenic
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