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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WT1
Single nucleotide variant
(splice donor variant +1 more)
WT1-related disorder
GPathogenic
LOC107982234, WT1
(V167D +1 more)
Single nucleotide variant
(missense variant +1 more)
Nephrotic syndrome, type 4
GLikely pathogenic