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rs7551188

From SNPedia

Orientationplus
Stabilizedplus
Make rs7551188(C;C)
Make rs7551188(C;T)
Make rs7551188(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position24946709
GeneRUNX3
is asnp
is mentioned by
dbSNPrs7551188
ebirs7551188
HLIrs7551188
Exacrs7551188
Varsomers7551188
Maprs7551188
PheGenIrs7551188
hapmaprs7551188
1000 genomesrs7551188
hgdprs7551188
ensemblrs7551188
gopubmedrs7551188
geneviewrs7551188
scholarrs7551188
googlers7551188
pharmgkbrs7551188
gwascentralrs7551188
openSNPrs7551188
23andMers7551188
23andMe allrs7551188
SNP Nexus

SNPshotrs7551188
SNPdbers7551188
MSV3drs7551188
GWAS Ctlgrs7551188
GMAF0.4844
Max Magnitude
? (C;C) (C;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 T
P-val 9E-6
Odds Ratio 1.18 [1.10-1.28]