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

rs6990917

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6990917(C;C)
Make rs6990917(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position67887142
is asnp
is mentioned by
dbSNPrs6990917
ebirs6990917
HLIrs6990917
Exacrs6990917
Varsomers6990917
Maprs6990917
PheGenIrs6990917
hapmaprs6990917
1000 genomesrs6990917
hgdprs6990917
ensemblrs6990917
gopubmedrs6990917
geneviewrs6990917
scholarrs6990917
googlers6990917
pharmgkbrs6990917
gwascentralrs6990917
openSNPrs6990917
23andMers6990917
23andMe allrs6990917
SNP Nexus

SNPshotrs6990917
SNPdbers6990917
MSV3drs6990917
GWAS Ctlgrs6990917
GMAF0.07254
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 0.000002
Odds Ratio None None