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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SERPINC1
(V391A +6 more)
Single nucleotide variant
(missense variant)
Stroke disorder
GUncertain significance
SERPINC1
(I143V +2 more)
Single nucleotide variant
(missense variant +1 more)
Stroke disorder
GUncertain significance