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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AXDND1, NPHS2
(V290M +1 more)
Single nucleotide variant
(missense variant +1 more)
NPHS2-related condition
+2 more
GConflicting classifications of pathogenicity
NPHS2
Single nucleotide variant
(intron variant +1 more)
Idiopathic nephrotic syndrome
+2 more
GPathogenic/Likely pathogenic
NPHS2
(P20L)
Single nucleotide variant
(missense variant)
Focal segmental glomerulosclerosis
+5 more
GConflicting classifications of pathogenicity
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