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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INF2
(K169E)
Single nucleotide variant
(missense variant)
Glomerulopathy with fibronectin deposits 2
GUncertain significance
INF2
(K407N)
Single nucleotide variant
(missense variant)
Focal segmental glomerulosclerosis 5
GUncertain significance