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rs7798500

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs7798500(A;G)
Make rs7798500(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position107021638
is asnp
is mentioned by
dbSNPrs7798500
ebirs7798500
HLIrs7798500
Exacrs7798500
Varsomers7798500
Maprs7798500
PheGenIrs7798500
hapmaprs7798500
1000 genomesrs7798500
hgdprs7798500
ensemblrs7798500
gopubmedrs7798500
geneviewrs7798500
scholarrs7798500
googlers7798500
pharmgkbrs7798500
gwascentralrs7798500
openSNPrs7798500
23andMers7798500
23andMe allrs7798500
SNP Nexus

SNPshotrs7798500
SNPdbers7798500
MSV3drs7798500
GWAS Ctlgrs7798500
GMAF0.1382
Max Magnitude0
? (A;A) (A;G) (G;G) 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 0.000006
Odds Ratio None None