Have questions? Visit https://www.reddit.com/r/SNPedia

rs415890

From SNPedia

Orientationplus
Stabilizedplus
Make rs415890(C;C)
Make rs415890(C;G)
Make rs415890(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position166993145
is asnp
is mentioned by
dbSNPrs415890
ebirs415890
HLIrs415890
Exacrs415890
Varsomers415890
Maprs415890
PheGenIrs415890
hapmaprs415890
1000 genomesrs415890
hgdprs415890
ensemblrs415890
gopubmedrs415890
geneviewrs415890
scholarrs415890
googlers415890
pharmgkbrs415890
gwascentralrs415890
openSNPrs415890
23andMers415890
23andMe allrs415890
SNP Nexus

SNPshotrs415890
SNPdbers415890
MSV3drs415890
GWAS Ctlgrs415890
GMAF0.3935
Max Magnitude
? (C;C) (C;G) (G;G) 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 C
P-val 3E-12
Odds Ratio 1.17 [1.12-1.22]