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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NETO2
(S449T +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
ABCC11, ABCC12
+9 more
Duplication
Glycogen storage disease IXb
GUncertain significance