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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F9
(A26T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
F9
(P159L +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
F9
(L372P +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely pathogenic
F9
(R346Q +1 more)
Single nucleotide variant
(missense variant)
Thrombus
+1 more
GUncertain significance
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