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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDR73
(G201E)
Single nucleotide variant
(missense variant +1 more)
Galloway-Mowat syndrome 1
GUncertain significance
WDR73
(D118E)
Single nucleotide variant
(missense variant +1 more)
Galloway-Mowat syndrome 1
+1 more
GConflicting classifications of pathogenicity
WDR73
(R96K)
Single nucleotide variant
(missense variant +1 more)
Galloway-Mowat syndrome 1
+1 more
GPathogenic/Likely pathogenic
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