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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC6A3
(A331P)
Single nucleotide variant
(missense variant)
Classic dopamine transporter deficiency syndrome
GUncertain significance
SLC6A3
(R219H)
Single nucleotide variant
(missense variant)
Classic dopamine transporter deficiency syndrome
GUncertain significance