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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NPHS2
(R229Q)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
TTC21B-AS1, TTC21B
(P209L)
Single nucleotide variant
(missense variant)
Asphyxiating thoracic dystrophy 4
+7 more
GPathogenic/Likely pathogenic
TRPC6
(R175W)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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