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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNFAIP3
(R87Q)
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome, familial, Behcet-like 1
GUncertain significance
TNFAIP3
(H368Y)
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome, familial, Behcet-like 1
GUncertain significance