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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IL7R
(E79*)
Single nucleotide variant
(nonsense +1 more)
Immunodeficiency 104
GLikely pathogenic
IL7R
(S105N)
Single nucleotide variant
(missense variant +1 more)
Immunodeficiency 104
GLikely benign
IL7R
(K289fs)
Deletion
(frameshift variant +1 more)
Immunodeficiency 104
GUncertain significance
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