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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SERPINC1
(F117C +2 more)
Single nucleotide variant
(missense variant)
Hereditary antithrombin deficiency
GUncertain significance
SERPINC1
(R79H +2 more)
Single nucleotide variant
(missense variant)
Hereditary antithrombin deficiency
GPathogenic
SERPINC1
(P73L +2 more)
Single nucleotide variant
(missense variant)
Hereditary antithrombin deficiency
GPathogenic
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