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rs7517810

From SNPedia

Orientationplus
Stabilizedplus
Make rs7517810(C;C)
Make rs7517810(C;T)
Make rs7517810(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position172884320
is asnp
is mentioned by
dbSNPrs7517810
ebirs7517810
HLIrs7517810
Exacrs7517810
Varsomers7517810
Maprs7517810
PheGenIrs7517810
hapmaprs7517810
1000 genomesrs7517810
hgdprs7517810
ensemblrs7517810
gopubmedrs7517810
geneviewrs7517810
scholarrs7517810
googlers7517810
pharmgkbrs7517810
gwascentralrs7517810
openSNPrs7517810
23andMers7517810
23andMe allrs7517810
SNP Nexus

SNPshotrs7517810
SNPdbers7517810
MSV3drs7517810
GWAS Ctlgrs7517810
GMAF0.4481
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 T
P-val 2E-15
Odds Ratio 1.22 [1.16-1.28]