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rs4569005

From SNPedia

Orientationplus
Stabilizedplus
Make rs4569005(C;C)
Make rs4569005(C;T)
Make rs4569005(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position21037185
GeneNELL1
is asnp
is mentioned by
dbSNPrs4569005
ebirs4569005
HLIrs4569005
Exacrs4569005
Varsomers4569005
Maprs4569005
PheGenIrs4569005
hapmaprs4569005
1000 genomesrs4569005
hgdprs4569005
ensemblrs4569005
gopubmedrs4569005
geneviewrs4569005
scholarrs4569005
googlers4569005
pharmgkbrs4569005
gwascentralrs4569005
openSNPrs4569005
23andMers4569005
23andMe allrs4569005
SNP Nexus

SNPshotrs4569005
SNPdbers4569005
MSV3drs4569005
GWAS Ctlgrs4569005
GMAF0.1552
Max Magnitude
? (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 0.000005
Odds Ratio None None