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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIK3R5
(R761W +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PIK3R5
(V211I)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
+1 more
GUncertain significance