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rs1456893

From SNPedia

Orientationplus
Stabilizedplus
Make rs1456893(A;A)
Make rs1456893(A;G)
Make rs1456893(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position50230076
is asnp
is mentioned by
dbSNPrs1456893
ebirs1456893
HLIrs1456893
Exacrs1456893
Varsomers1456893
Maprs1456893
PheGenIrs1456893
hapmaprs1456893
1000 genomesrs1456893
hgdprs1456893
ensemblrs1456893
gopubmedrs1456893
geneviewrs1456893
scholarrs1456893
googlers1456893
pharmgkbrs1456893
gwascentralrs1456893
openSNPrs1456893
23andMers1456893
23andMe allrs1456893
SNP Nexus

SNPshotrs1456893
SNPdbers1456893
MSV3drs1456893
GWAS Ctlgrs1456893
GMAF0.3857
Max Magnitude
? (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 A
P-val 5.0000000000000001E-9
Odds Ratio 1.20 [NR]

DeCode reports that rs1456893 is associated with susceptibility to Crohn's disease. [PMID 18587394OA-icon.png]


[PMID 19068216OA-icon.png] Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.


[PMID 21304977OA-icon.png] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.


[PMID 21830272OA-icon.png] Distinct and overlapping genetic loci in Crohn's disease and ulcerative colitis: correlations with pathogenesis.


GET Evidence
rs1456893
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.71875
summary