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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC6A3
Single nucleotide variant
(synonymous variant)
Parkinsonism-dystonia, infantile
+2 more
GBenign
SLC6A3
(A559V)
Single nucleotide variant
(missense variant)
Parkinsonism-dystonia, infantile
+4 more
GUncertain significance
SLC6A3
Single nucleotide variant
(synonymous variant)
Parkinsonism-dystonia, infantile
+2 more
GConflicting classifications of pathogenicity
SLC6A3
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC6A3
Single nucleotide variant
(synonymous variant)
Parkinsonism-dystonia, infantile
+3 more
GBenign
SLC6A3
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
SLC6A3
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC6A3
Single nucleotide variant
(synonymous variant)
Parkinsonism-dystonia, infantile
+1 more
GConflicting classifications of pathogenicity
SLC6A3
(A57V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC6A3
(T48S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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