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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDR19
(T101fs +1 more)
Duplication
(frameshift variant)
WDR19-related disorder
+4 more
GConflicting classifications of pathogenicity
WDR19
(L275R +1 more)
Single nucleotide variant
(missense variant)
Nephronophthisis 13
GUncertain significance
WDR19
(R1178Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
WDR19
Copy number loss
Nephronophthisis 13
GPathogenic
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