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Items: 30

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AASDHPPT, ABCG4
+1199 more
Copy number gain
See cases
GPathogenic
DRD2
Single nucleotide variant
(3 prime UTR variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
DRD2
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign
DRD2
(S311C +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
Dystonic disorder
+1 more
GBenign/Likely benign
DRD2
Duplication
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(synonymous variant)
Dystonic disorder
+1 more
GBenign
DRD2
Single nucleotide variant
(intron variant)
not provided
GBenign
DRD2
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign
DRD2
Duplication
Dystonic disorder
+1 more
GBenign
DRD2
Single nucleotide variant
Dystonic disorder
+2 more
GBenign
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