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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F13A1
(L236R)
Single nucleotide variant
(missense variant)
Factor XIII, A subunit, deficiency of
GUncertain significance
F13A1
(I154fs)
Insertion
(frameshift variant)
Factor XIII, A subunit, deficiency of
GPathogenic