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rs9469003

From SNPedia

Orientationplus
Stabilizedplus
Make rs9469003(C;C)
Make rs9469003(C;T)
Make rs9469003(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31440051
GeneLINC01149
is asnp
is mentioned by
dbSNPrs9469003
ebirs9469003
HLIrs9469003
Exacrs9469003
Varsomers9469003
Maprs9469003
PheGenIrs9469003
hapmaprs9469003
1000 genomesrs9469003
hgdprs9469003
ensemblrs9469003
gopubmedrs9469003
geneviewrs9469003
scholarrs9469003
googlers9469003
pharmgkbrs9469003
gwascentralrs9469003
openSNPrs9469003
23andMers9469003
23andMe allrs9469003
SNP Nexus

SNPshotrs9469003
SNPdbers9469003
MSV3drs9469003
GWAS Ctlgrs9469003
GMAF0.2406
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21801394OA-icon.png]
Trait
Title Genome-Wide Association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.
Risk Allele C
P-val 2E-9
Odds Ratio 1.7300 [1.44-2.08]


[PMID 26049586] A human leukocyte antigen locus haplotype confers risk for allopurinol-related adverse effects in Caucasian patients with gout


[PMID 26083016] Accuracy of SNPs to predict risk of HLA alleles associated with drug-induced hypersensitivity events across racial groups