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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL4A4
(G795R)
Single nucleotide variant
(missense variant)
Polycystic kidney disease
GPathogenic
PKHD1
(T36M)
Single nucleotide variant
(missense variant)
Autosomal recessive polycystic kidney disease
+7 more
GPathogenic/Likely pathogenic