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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NUP93
(R402W +1 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 12
GUncertain significance
NUP93
(G591V +1 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 12
+1 more
GPathogenic/Likely pathogenic
NUP93
Single nucleotide variant
(synonymous variant)
Nephrotic syndrome, type 12
GUncertain significance
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