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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAC1
(T17S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
RAC1
(N26S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity