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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CD3G, LOC126861358
(V131F)
Indel
(missense variant)
Combined immunodeficiency due to CD3gamma deficiency
GBenign
CD3G, LOC126861358
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
CD3G, LOC126861358
(V131F)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
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