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rs740495

From SNPedia

Orientationminus
Stabilizedminus
Make rs740495(C;C)
Make rs740495(C;T)
Make rs740495(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position1124836
GeneSBNO2
is asnp
is mentioned by
dbSNPrs740495
ebirs740495
HLIrs740495
Exacrs740495
Varsomers740495
Maprs740495
PheGenIrs740495
hapmaprs740495
1000 genomesrs740495
hgdprs740495
ensemblrs740495
gopubmedrs740495
geneviewrs740495
scholarrs740495
googlers740495
pharmgkbrs740495
gwascentralrs740495
openSNPrs740495
23andMers740495
23andMe allrs740495
SNP Nexus

SNPshotrs740495
SNPdbers740495
MSV3drs740495
GWAS Ctlgrs740495
GMAF0.3852
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait Crohn's disease
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
Risk Allele G
P-val 8E-12
Odds Ratio 1.16 [1.10-1.21]