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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
XIAP
(R62W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
XIAP
(E282K)
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome
+3 more
GUncertain significance
XIAP
(Q423P)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GBenign
XIAP
Single nucleotide variant
(3 prime UTR variant +1 more)
X-linked lymphoproliferative disease due to XIAP deficiency
+1 more
GBenign
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