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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129992813, PKD2
(E102del)
Microsatellite
(inframe_deletion +1 more)
Autosomal dominant polycystic kidney disease
GBenign
PKD2
(F482C)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity