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rs3853240

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs3853240(C;C)
Make rs3853240(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position166891185
is asnp
is mentioned by
dbSNPrs3853240
ebirs3853240
HLIrs3853240
Exacrs3853240
Varsomers3853240
Maprs3853240
PheGenIrs3853240
hapmaprs3853240
1000 genomesrs3853240
hgdprs3853240
ensemblrs3853240
gopubmedrs3853240
geneviewrs3853240
scholarrs3853240
googlers3853240
pharmgkbrs3853240
gwascentralrs3853240
openSNPrs3853240
23andMers3853240
23andMe allrs3853240
SNP Nexus

SNPshotrs3853240
SNPdbers3853240
MSV3drs3853240
GWAS Ctlgrs3853240
GMAF0.06612
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 0.000001
Odds Ratio None None