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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PKHD1
(L3485fs)
Duplication
(frameshift variant)
Polycystic kidney disease 4
+1 more
GPathogenic/Likely pathogenic
EFHC1, IL17A
+7 more
Copy number loss
Autosomal recessive polycystic kidney disease
GPathogenic