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Links from MedGen

Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DRD3
(P135H)
Single nucleotide variant
(missense variant)
Tremor, hereditary essential, 1
GUncertain significance
DRD3
(A38T)
Single nucleotide variant
(missense variant)
Tremor, hereditary essential, 1
GLikely benign
DRD3
(V136I)
Single nucleotide variant
(missense variant)
Tremor, hereditary essential, 1
GLikely benign
DRD3
Single nucleotide variant
(5 prime UTR variant +1 more)
Tremor, hereditary essential, 1
GBenign
DRD3
Single nucleotide variant
(5 prime UTR variant +1 more)
Tremor, hereditary essential, 1
GLikely benign
DRD3
Single nucleotide variant
(5 prime UTR variant +1 more)
Tremor, hereditary essential, 1
GLikely benign
DRD3
Single nucleotide variant
(5 prime UTR variant)
Tremor, hereditary essential, 1
GLikely benign
DRD3
Single nucleotide variant
(5 prime UTR variant)
Tremor, hereditary essential, 1
GLikely benign
DRD3
Single nucleotide variant
(synonymous variant)
Tremor, hereditary essential, 1
+1 more
GBenign
DRD3
(C231S)
Single nucleotide variant
(missense variant)
Tremor, hereditary essential, 1
+1 more
GLikely benign
DRD3
Single nucleotide variant
(synonymous variant +1 more)
Tremor, hereditary essential, 1
GBenign
DRD3
Single nucleotide variant
(synonymous variant)
Tremor, hereditary essential, 1
+1 more
GBenign
DRD3
Single nucleotide variant
(synonymous variant)
Tremor, hereditary essential, 1
+1 more
GBenign/Likely benign
DRD3
(G9S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
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