rs4906902
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs4906902(A;G) |
Make rs4906902(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 26774621 |
Gene | GABRB3 |
is a | snp |
is | mentioned by |
dbSNP | rs4906902 |
dbSNP (classic) | rs4906902 |
ClinGen | rs4906902 |
ebi | rs4906902 |
HLI | rs4906902 |
Exac | rs4906902 |
Gnomad | rs4906902 |
Varsome | rs4906902 |
LitVar | rs4906902 |
Map | rs4906902 |
PheGenI | rs4906902 |
Biobank | rs4906902 |
1000 genomes | rs4906902 |
hgdp | rs4906902 |
ensembl | rs4906902 |
geneview | rs4906902 |
scholar | rs4906902 |
rs4906902 | |
pharmgkb | rs4906902 |
gwascentral | rs4906902 |
openSNP | rs4906902 |
23andMe | rs4906902 |
SNPshot | rs4906902 |
SNPdbe | rs4906902 |
MSV3d | rs4906902 |
GWAS Ctlg | rs4906902 |
GMAF | 0.2062 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22765836] Effects on promoter activity of common SNPs in 5' region of GABRB3 exon 1A
[PMID 22082659] Promoter variants determine γ-aminobutyric acid homeostasis-related gene transcription in human epileptic hippocampi
[PMID 17215107] Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.
[PMID 21905019] Large candidate gene association study reveals genetic risk factors and therapeutic targets for fibromyalgia.
[PMID 25025424] Association Analysis of GABRB3 Promoter Variants with Heroin Dependence
[PMID 29196882] The GABRB3 Polymorphism and its Association with Schizophrenia.