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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SH2D1A
(D2G)
Single nucleotide variant
(missense variant)
X-linked lymphoproliferative disease due to SH2D1A deficiency
+1 more
GLikely pathogenic
SH2D1A
(W64*)
Single nucleotide variant
(nonsense)
X-linked lymphoproliferative disease due to SH2D1A deficiency
GPathogenic
SH2D1A
Single nucleotide variant
(stop lost)
X-linked lymphoproliferative disease due to SH2D1A deficiency
GLikely pathogenic
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