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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNFAIP3
(E366*)
Single nucleotide variant
(nonsense)
Autoinflammatory syndrome, familial, Behcet-like 1
GLikely pathogenic
TNFAIP3
(A586V)
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome, familial, Behcet-like
+1 more
GUncertain significance
TNFAIP3
(R697K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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