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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NPHS1
(V187M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
NPHS1
(T172del)
Deletion
(inframe_deletion)
Finnish congenital nephrotic syndrome
+1 more
GConflicting classifications of pathogenicity