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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIK3CD
(P173H)
Single nucleotide variant
(missense variant)
Immunodeficiency 14
GUncertain significance
LOC126805612, PIK3CD
Deletion
(intron variant)
Immunodeficiency 14
GUncertain significance
PIK3CD
(E525K +2 more)
Single nucleotide variant
(missense variant)
Immunodeficiency 14
GPathogenic/Likely pathogenic
PIK3CD
(R898H +2 more)
Single nucleotide variant
(missense variant)
Immunodeficiency 14
GUncertain significance
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