rs17002253
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs17002253(C;C) |
Make rs17002253(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 76850192 |
is a | snp |
is | mentioned by |
dbSNP | rs17002253 |
dbSNP (classic) | rs17002253 |
ClinGen | rs17002253 |
ebi | rs17002253 |
HLI | rs17002253 |
Exac | rs17002253 |
Gnomad | rs17002253 |
Varsome | rs17002253 |
LitVar | rs17002253 |
Map | rs17002253 |
PheGenI | rs17002253 |
Biobank | rs17002253 |
1000 genomes | rs17002253 |
hgdp | rs17002253 |
ensembl | rs17002253 |
geneview | rs17002253 |
scholar | rs17002253 |
rs17002253 | |
pharmgkb | rs17002253 |
gwascentral | rs17002253 |
openSNP | rs17002253 |
23andMe | rs17002253 |
SNPshot | rs17002253 |
SNPdbe | rs17002253 |
MSV3d | rs17002253 |
GWAS Ctlg | rs17002253 |
GMAF | 0.09229 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22379998] |
Trait | |
Title | Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions. |
Risk Allele | |
P-val | 0.000007 |
Odds Ratio | None None |