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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAC2
(T182M)
Single nucleotide variant
(missense variant)
Neutrophil immunodeficiency syndrome
+1 more
GConflicting classifications of pathogenicity
RAC2
(F169L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
RAC2
(P99L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
RAC2
(P87S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
RAC2
(V14M)
Single nucleotide variant
(missense variant)
Neutrophil immunodeficiency syndrome
+1 more
GUncertain significance
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