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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F7
(P48S +1 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
+1 more
GUncertain significance
F7
Single nucleotide variant
(intron variant)
Congenital factor VII deficiency
Gnot provided