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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBC1D8B
(Q246H)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 20
GLikely pathogenic
TBC1D8B
(F291S)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 20
GLikely pathogenic