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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INF2
(E184K)
Single nucleotide variant
(missense variant)
Focal segmental glomerulosclerosis 5
+1 more
GPathogenic
INF2
(H802Q)
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease dominant intermediate E
GUncertain significance