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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129992813, PKD2
(Q61*)
Single nucleotide variant
(nonsense +1 more)
not provided
+1 more
GPathogenic/Likely pathogenic
LOC129992813, PKD2
(V103M)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance