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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IL2RG
(I273fs)
Microsatellite
(frameshift variant)
X-linked severe combined immunodeficiency
GPathogenic
IL2RG
(E109K)
Single nucleotide variant
(missense variant)
X-linked severe combined immunodeficiency
GBenign
LOC126863274, IL2RG
Single nucleotide variant
(synonymous variant)
IL2RG-related condition
+2 more
GBenign/Likely benign
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