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rs76418789

From SNPedia

Orientationplus
Stabilizedplus
Make rs76418789(A;A)
Make rs76418789(A;G)
Make rs76418789(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position67182913
GeneIL23R
is asnp
is mentioned by
dbSNPrs76418789
ebirs76418789
HLIrs76418789
Exacrs76418789
Varsomers76418789
Maprs76418789
PheGenIrs76418789
hapmaprs76418789
1000 genomesrs76418789
hgdprs76418789
ensemblrs76418789
gopubmedrs76418789
geneviewrs76418789
scholarrs76418789
googlers76418789
pharmgkbrs76418789
gwascentralrs76418789
openSNPrs76418789
23andMers76418789
23andMe allrs76418789
SNP Nexus

SNPshotrs76418789
SNPdbers76418789
MSV3drs76418789
GWAS Ctlgrs76418789
GMAF0.01974
Max Magnitude
GWAS snp
PMID [PMID 23850713]
Trait Crohn's disease
Title Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.
Risk Allele G
P-val 2E-10
Odds Ratio 2.06 [1.64-2.58]

[PMID 26398853] Identification of Ten Additional Susceptibility Loci for Ulcerative Colitis Through Immunochip Analysis in Koreans