rs7798500
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs7798500(A;G) |
Make rs7798500(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 107021638 |
is a | snp |
is | mentioned by |
dbSNP | rs7798500 |
dbSNP (classic) | rs7798500 |
ClinGen | rs7798500 |
ebi | rs7798500 |
HLI | rs7798500 |
Exac | rs7798500 |
Gnomad | rs7798500 |
Varsome | rs7798500 |
LitVar | rs7798500 |
Map | rs7798500 |
PheGenI | rs7798500 |
Biobank | rs7798500 |
1000 genomes | rs7798500 |
hgdp | rs7798500 |
ensembl | rs7798500 |
geneview | rs7798500 |
scholar | rs7798500 |
rs7798500 | |
pharmgkb | rs7798500 |
gwascentral | rs7798500 |
openSNP | rs7798500 |
23andMe | rs7798500 |
SNPshot | rs7798500 |
SNPdbe | rs7798500 |
MSV3d | rs7798500 |
GWAS Ctlg | rs7798500 |
GMAF | 0.1382 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 0.000006 |
Odds Ratio | None None |