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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DRD5, SLC2A9
Single nucleotide variant
(synonymous variant)
Schizophrenia
+1 more
GUncertain significance
DRD5, SLC2A9
Single nucleotide variant
(3 prime UTR variant)
Hereditary attention deficit-hyperactivity disorder
+1 more
GConflicting classifications of pathogenicity