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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INF2
(I118N)
Single nucleotide variant
(missense variant)
Focal segmental glomerulosclerosis 5
GLikely pathogenic
INF2
(F178V)
Single nucleotide variant
(missense variant)
Nephrotic syndrome
GLikely pathogenic
INF2
(V181G)
Single nucleotide variant
(missense variant)
Focal segmental glomerulosclerosis
GPathogenic
INF2
(R218Q)
Single nucleotide variant
(missense variant)
Focal segmental glomerulosclerosis 5
+4 more
GPathogenic/Likely pathogenic
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