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rs17002253

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17002253(C;C)
Make rs17002253(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position76850192
is asnp
is mentioned by
dbSNPrs17002253
ebirs17002253
HLIrs17002253
Exacrs17002253
Varsomers17002253
Maprs17002253
PheGenIrs17002253
hapmaprs17002253
1000 genomesrs17002253
hgdprs17002253
ensemblrs17002253
gopubmedrs17002253
geneviewrs17002253
scholarrs17002253
googlers17002253
pharmgkbrs17002253
gwascentralrs17002253
openSNPrs17002253
23andMers17002253
23andMe allrs17002253
SNP Nexus

SNPshotrs17002253
SNPdbers17002253
MSV3drs17002253
GWAS Ctlgrs17002253
GMAF0.09229
Max Magnitude0
? (C;C) (C;T) (T;T) 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 0.000007
Odds Ratio None None