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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNFRSF13B
(A181E)
Single nucleotide variant
(missense variant)
not specified
+5 more
GConflicting classifications of pathogenicity
TNFRSF13B
(C104R)
Single nucleotide variant
(missense variant)
Immunodeficiency, common variable, 2
+22 more
GConflicting classifications of pathogenicity; risk factor