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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ICOS
(G24V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ICOS
(I77V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ICOS
(I113V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ICOS
(Q134P)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ICOS
(K167M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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