Have questions? Visit https://www.reddit.com/r/SNPedia

rs183266

From SNPedia

Orientationplus
Stabilizedplus
Make rs183266(A;A)
Make rs183266(A;C)
Make rs183266(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position77031632
is asnp
is mentioned by
dbSNPrs183266
ebirs183266
HLIrs183266
Exacrs183266
Varsomers183266
Maprs183266
PheGenIrs183266
hapmaprs183266
1000 genomesrs183266
hgdprs183266
ensemblrs183266
gopubmedrs183266
geneviewrs183266
scholarrs183266
googlers183266
pharmgkbrs183266
gwascentralrs183266
openSNPrs183266
23andMers183266
23andMe allrs183266
SNP Nexus

SNPshotrs183266
SNPdbers183266
MSV3drs183266
GWAS Ctlgrs183266
GMAF0.1524
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22379998OA-icon.png]
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