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

rs9268877

From SNPedia

Orientationplus
Stabilizedplus
Make rs9268877(A;A)
Make rs9268877(A;G)
Make rs9268877(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32463370
is asnp
is mentioned by
dbSNPrs9268877
ebirs9268877
HLIrs9268877
Exacrs9268877
Varsomers9268877
Maprs9268877
PheGenIrs9268877
hapmaprs9268877
1000 genomesrs9268877
hgdprs9268877
ensemblrs9268877
gopubmedrs9268877
geneviewrs9268877
scholarrs9268877
googlers9268877
pharmgkbrs9268877
gwascentralrs9268877
openSNPrs9268877
23andMers9268877
23andMe allrs9268877
SNP Nexus

SNPshotrs9268877
SNPdbers9268877
MSV3drs9268877
GWAS Ctlgrs9268877
GMAF0.4164
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18836448]
Trait Ulcerative colitis
Title Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility
Risk Allele T
P-val 5.9999999999999997E-18
Odds Ratio 1.45 [1.33-1.58]
OMIM604519
DescINFLAMMATORY BOWEL DISEASE 3; IBD3
Variant
Relatedalso


GWAS snp
PMID [PMID 19915572OA-icon.png]
Trait Ulcerative colitis
Title Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
Risk Allele
P-val 4E-23
Odds Ratio NR NR



[PMID 17660530] Risk alleles for multiple sclerosis identified by a genomewide study.


[PMID 19122664OA-icon.png] Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.


[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.


[PMID 20546594OA-icon.png] An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings.


GET Evidence
rs9268877
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.614754
summary