rs6275
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs6275(C;C) |
Make rs6275(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 113412755 |
Gene | DRD2 |
is a | snp |
is | mentioned by |
dbSNP | rs6275 |
dbSNP (classic) | rs6275 |
ClinGen | rs6275 |
ebi | rs6275 |
HLI | rs6275 |
Exac | rs6275 |
Gnomad | rs6275 |
Varsome | rs6275 |
LitVar | rs6275 |
Map | rs6275 |
PheGenI | rs6275 |
Biobank | rs6275 |
1000 genomes | rs6275 |
hgdp | rs6275 |
ensembl | rs6275 |
geneview | rs6275 |
scholar | rs6275 |
rs6275 | |
pharmgkb | rs6275 |
gwascentral | rs6275 |
openSNP | rs6275 |
23andMe | rs6275 |
SNPshot | rs6275 |
SNPdbe | rs6275 |
MSV3d | rs6275 |
GWAS Ctlg | rs6275 |
GMAF | 0.4729 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19207030] rs6275/DRD2 and rs4680/COMT useful in predicting disease risk among schizophrenia patients
See also rs6277.
[PMID 19373123] Genetic variants altering dopamine D2 receptor expression or function modulate the risk of opiate addiction and the dosage requirements of methadone substitution
[PMID 18838251] Genetic study of eight AKT1 gene polymorphisms and their interaction with DRD2 gene polymorphisms in tardive dyskinesia
[PMID 19512960] Genetic diagnostics of functional variants of the human dopamine D2 receptor gene
[PMID 21095016] Association of DRD2 and ANKK1 polymorphisms with prolactin increase in olanzapine-treated women
[PMID 16867246] Association of DRD2 polymorphisms and chlorpromazine-induced extrapyramidal syndrome in Chinese schizophrenic patients.
[PMID 18077373] Polymorphisms in human dopamine D2 receptor gene affect gene expression, splicing, and neuronal activity during working memory.
[PMID 18154681] A lesson not learned: allele misassignment.
[PMID 18305461] Association between ADORA2A and DRD2 polymorphisms and caffeine-induced anxiety.
[PMID 18477981] [The association study of the DRD2 gene C939T polymorphism and schizophrenia.]
[PMID 18698231] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.
[PMID 18829695] Functional variants of the dopamine receptor D2 gene modulate prefronto-striatal phenotypes in schizophrenia.
[PMID 19197363] A genome-wide investigation of SNPs and CNVs in schizophrenia.
[PMID 19590515] Association between dopaminergic genes (SLC6A3 and DRD2) and stuttering among Han Chinese.
[PMID 19772578] Two-stage case-control association study of dopamine-related genes and migraine.
[PMID 19911060] Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint.
[PMID 19913597] An association study of DRD2 gene polymorphisms with schizophrenia in a Chinese Han population.
[PMID 20191112] The Genetics of Anorexia Nervosa: Current Findings and Future Perspectives.
[PMID 21354244] The role of dopamine transporter (SLC6A3) and dopamine D2 receptor/ankyrin repeat and kinase domain containing 1 (DRD2/ANKK1) gene polymorphisms in personality traits.
[PMID 22290307] Predictive index for the onset of medication overuse headache in migraine patients.
[PMID 22615781] Candidate gene-based association study of antipsychotic-induced movement disorders in long-stay psychiatric patients: a prospective study
[PMID 22875483] Identification of a novel ANKK1 and other dopaminergic (DRD2 and DBH) gene variants in migraine susceptibility.
[PMID 22970887] The association between DRD2/ANKK1 and genetically informed measures of alcohol use and problems.
[PMID 26370377] Recurrent miscarriage is associated with the dopamine receptor (DRD2) genotype
[PMID 27254804] Dopamine 2 Receptor Genes Are Associated with Raised Blood Glucose in Schizophrenia.
ClinVar | |
---|---|
Risk | rs6275(C;C) |
Alt | rs6275(C;C) |
Reference | Rs6275(T;T) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | DRD2 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000011.9:g.113283477A>G |
CLNSRC | |
CLNACC | RCV000242384.1, |