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rs3094188

From SNPedia

Orientationminus
Stabilizedminus
Make rs3094188(G;G)
Make rs3094188(G;T)
Make rs3094188(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31174468
GenePSORS1C3
is asnp
is mentioned by
dbSNPrs3094188
ebirs3094188
HLIrs3094188
Exacrs3094188
Varsomers3094188
Maprs3094188
PheGenIrs3094188
hapmaprs3094188
1000 genomesrs3094188
hgdprs3094188
ensemblrs3094188
gopubmedrs3094188
geneviewrs3094188
scholarrs3094188
googlers3094188
pharmgkbrs3094188
gwascentralrs3094188
openSNPrs3094188
23andMers3094188
23andMe allrs3094188
SNP Nexus

SNPshotrs3094188
SNPdbers3094188
MSV3drs3094188
GWAS Ctlgrs3094188
GMAF0.281
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23266558]
Trait Crohn's disease
Title A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population.
Risk Allele C
P-val 7E-7
Odds Ratio 1.61 [1.33-1.94]


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