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rs2844665

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2844665(A;A)
Make rs2844665(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31039078
is asnp
is mentioned by
dbSNPrs2844665
ebirs2844665
HLIrs2844665
Exacrs2844665
Varsomers2844665
Maprs2844665
PheGenIrs2844665
hapmaprs2844665
1000 genomesrs2844665
hgdprs2844665
ensemblrs2844665
gopubmedrs2844665
geneviewrs2844665
scholarrs2844665
googlers2844665
pharmgkbrs2844665
gwascentralrs2844665
openSNPrs2844665
23andMers2844665
23andMe allrs2844665
SNP Nexus

SNPshotrs2844665
SNPdbers2844665
MSV3drs2844665
GWAS Ctlgrs2844665
GMAF0.3843
Max Magnitude0
? (A;A) (A;G) (G;G) 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 3E-7
Odds Ratio 1.5400 [1.30-1.82]


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