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rs7746082

From SNPedia

Orientationplus
Stabilizedplus
Make rs7746082(C;C)
Make rs7746082(C;G)
Make rs7746082(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position105987394
is asnp
is mentioned by
dbSNPrs7746082
ebirs7746082
HLIrs7746082
Exacrs7746082
Varsomers7746082
Maprs7746082
PheGenIrs7746082
hapmaprs7746082
1000 genomesrs7746082
hgdprs7746082
ensemblrs7746082
gopubmedrs7746082
geneviewrs7746082
scholarrs7746082
googlers7746082
pharmgkbrs7746082
gwascentralrs7746082
openSNPrs7746082
23andMers7746082
23andMe allrs7746082
SNP Nexus

SNPshotrs7746082
SNPdbers7746082
MSV3drs7746082
GWAS Ctlgrs7746082
GMAF0.1345
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS
SNP rs7746082
PubMedID [PMID 18587394OA-icon.png]
Condition Crohn's disease
Gene Unknown
Risk Allele C
pValue 2.00E-010
OR 1.17
95% CI



DeCode reports that rs7746082 is associated with susceptibility to Crohn's disease. [PMID 18587394OA-icon.png]


[PMID 21752155OA-icon.png] Genetic susceptibility to inflammation and colonic transit in lower functional gastrointestinal disorders: preliminary analysis

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


GET Evidence
rs7746082
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.125
summary