rs285406
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs285406(A;A) |
Make rs285406(A;G) |
Make rs285406(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 86012784 |
is a | snp |
is | mentioned by |
dbSNP | rs285406 |
dbSNP (classic) | rs285406 |
ClinGen | rs285406 |
ebi | rs285406 |
HLI | rs285406 |
Exac | rs285406 |
Gnomad | rs285406 |
Varsome | rs285406 |
LitVar | rs285406 |
Map | rs285406 |
PheGenI | rs285406 |
Biobank | rs285406 |
1000 genomes | rs285406 |
hgdp | rs285406 |
ensembl | rs285406 |
geneview | rs285406 |
scholar | rs285406 |
rs285406 | |
pharmgkb | rs285406 |
gwascentral | rs285406 |
openSNP | rs285406 |
23andMe | rs285406 |
SNPshot | rs285406 |
SNPdbe | rs285406 |
MSV3d | rs285406 |
GWAS Ctlg | rs285406 |
GMAF | 0.03857 |
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 | 0.000005 |
Odds Ratio | None None |