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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INF2
(R56H)
Single nucleotide variant
(missense variant)
Focal segmental glomerulosclerosis 5
GLikely pathogenic
INF2
(C104R)
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease dominant intermediate E
+2 more
GConflicting classifications of pathogenicity