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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PNP
(G51S)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
PNP
(R58*)
Indel
(nonsense)
Purine-nucleoside phosphorylase deficiency
GPathogenic
PNP
(R58*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
PNP
Single nucleotide variant
(intron variant)
Severe combined immunodeficiency disease
+1 more
GPathogenic/Likely pathogenic
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