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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
XIAP
Deletion
(splice acceptor variant +2 more)
X-linked lymphoproliferative disease due to XIAP deficiency
GLikely pathogenic
XIAP
(G188R)
Single nucleotide variant
(missense variant)
X-linked lymphoproliferative disease due to XIAP deficiency
+2 more
GConflicting classifications of pathogenicity
XIAP
(T486fs)
Microsatellite
(frameshift variant +1 more)
X-linked lymphoproliferative disease due to XIAP deficiency
GUncertain significance
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