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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NUP107
(M101I +1 more)
Single nucleotide variant
(missense variant)
Galloway-Mowat syndrome 7
+1 more
GPathogenic
NUP107
(Y889C +1 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 11
GLikely pathogenic