Rs11747270

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Orientationplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs11747270(A;G)
Make rs11747270(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position150879305
is asnp
is mentioned by
dbSNPrs11747270
Exacrs11747270
PheGenIrs11747270
nextbiors11747270
hapmaprs11747270
1000 genomesrs11747270
hgdprs11747270
ensemblrs11747270
gopubmedrs11747270
geneviewrs11747270
scholarrs11747270
googlers11747270
pharmgkbrs11747270
gwascentralrs11747270
openSNPrs11747270
23andMers11747270
23andMe allrs11747270
SNP Nexus

SNPshotrs11747270
SNPdbers11747270
MSV3drs11747270
GMAF0.2828
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18587394OA-icon.png]
Trait Crohn's disease
Title Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease
Risk Allele G
P-val 2.9999999999999999E-16
Odds Ratio 1.33 [NR]
OMIM612278
DescINFLAMMATORY BOWEL DISEASE 19; IBD19
Variant
Relatedalso
[PMID 19557189OA-icon.png] Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.


[PMID 20106866OA-icon.png] Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.


[PMID 22065112] The JAK2 variant rs10758669 in Crohn's disease: altering the intestinal barrier as one mechanism of action.


GET Evidence
rs11747270
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.285714
summary