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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGDIA
(T182A)
Single nucleotide variant
(3 prime UTR variant +3 more)
Nephrotic syndrome, type 8
GUncertain significance
ARHGDIA, LOC130061973
(E130D)
Single nucleotide variant
(missense variant +1 more)
Nephrotic syndrome, type 8
+1 more
GConflicting classifications of pathogenicity