rs1800443
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 3.5 | Rare DRD4 polymorphism |
(G;T) | 3 | Uncommon DRD4 polymorphism |
(T;T) | 0 | common in clinvar |
Reference | GRCh37 37.1/131 |
Chromosome | 11 |
Position | 639830 |
Gene | DRD4 |
is a | snp |
is | mentioned by |
dbSNP | rs1800443 |
dbSNP (classic) | rs1800443 |
ClinGen | rs1800443 |
ebi | rs1800443 |
HLI | rs1800443 |
Exac | rs1800443 |
Gnomad | rs1800443 |
Varsome | rs1800443 |
LitVar | rs1800443 |
Map | rs1800443 |
PheGenI | rs1800443 |
Biobank | rs1800443 |
1000 genomes | rs1800443 |
hgdp | rs1800443 |
ensembl | rs1800443 |
geneview | rs1800443 |
scholar | rs1800443 |
rs1800443 | |
pharmgkb | rs1800443 |
gwascentral | rs1800443 |
openSNP | rs1800443 |
23andMe | rs1800443 |
SNPshot | rs1800443 |
SNPdbe | rs1800443 |
MSV3d | rs1800443 |
GWAS Ctlg | rs1800443 |
GMAF | 0.01194 |
Max Magnitude | 3.5 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | Rs1800443(G;G) |
Alt | Rs1800443(G;G) |
Reference | Rs1800443(T;T) |
Significance | Non-pathogenic |
Disease | DOPAMINE RECEPTOR D4 POLYMORPHISM |
Variation | info |
Gene | DRD4 |
CLNDBN | DOPAMINE RECEPTOR D4 POLYMORPHISM |
Reversed | 0 |
HGVS | NC_000011.9:g.639830T>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000018255.3, |
[PMID 19584173] Kininogen gene (KNG) variation has a consistent effect on aldosterone response to antihypertensive drug therapy: the GERA study.