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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129992813, PKD2
(R28P)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GBenign
LOC129992813, PKD2
Microsatellite
(inframe_insertion +1 more)
PKD2-related condition
+4 more
GBenign/Likely benign
LOC129992813, PKD2
Single nucleotide variant
(synonymous variant +1 more)
PKD2-related condition
+4 more
GBenign
LOC129992813, PKD2
(A190T)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant polycystic kidney disease
+3 more
GBenign
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