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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AXDND1, NPHS2
(G273W +1 more)
Single nucleotide variant
(missense variant +1 more)
Proteinuria
GUncertain significance
NPHS2
(R229Q)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
NPHS2
(P118L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
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