rs8083432
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8083432(A;A) |
Make rs8083432(A;C) |
Make rs8083432(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 25151396 |
Gene | ZNF521 |
is a | snp |
is | mentioned by |
dbSNP | rs8083432 |
dbSNP (classic) | rs8083432 |
ClinGen | rs8083432 |
ebi | rs8083432 |
HLI | rs8083432 |
Exac | rs8083432 |
Gnomad | rs8083432 |
Varsome | rs8083432 |
LitVar | rs8083432 |
Map | rs8083432 |
PheGenI | rs8083432 |
Biobank | rs8083432 |
1000 genomes | rs8083432 |
hgdp | rs8083432 |
ensembl | rs8083432 |
geneview | rs8083432 |
scholar | rs8083432 |
rs8083432 | |
pharmgkb | rs8083432 |
gwascentral | rs8083432 |
openSNP | rs8083432 |
23andMe | rs8083432 |
SNPshot | rs8083432 |
SNPdbe | rs8083432 |
MSV3d | rs8083432 |
GWAS Ctlg | rs8083432 |
GMAF | 0.1997 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 |