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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDR73
(R256Q)
Single nucleotide variant
(missense variant +1 more)
Galloway-Mowat syndrome 1
GLikely pathogenic
WDR73
(L98P)
Single nucleotide variant
(missense variant +1 more)
Galloway-Mowat syndrome 1
GLikely pathogenic