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

rs348594

From SNPedia

Orientationplus
Stabilizedplus
Make rs348594(A;A)
Make rs348594(A;G)
Make rs348594(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position40323836
is asnp
is mentioned by
dbSNPrs348594
ebirs348594
HLIrs348594
Exacrs348594
Varsomers348594
Maprs348594
PheGenIrs348594
hapmaprs348594
1000 genomesrs348594
hgdprs348594
ensemblrs348594
gopubmedrs348594
geneviewrs348594
scholarrs348594
googlers348594
pharmgkbrs348594
gwascentralrs348594
openSNPrs348594
23andMers348594
23andMe allrs348594
SNP Nexus

SNPshotrs348594
SNPdbers348594
MSV3drs348594
GWAS Ctlgrs348594
GMAF0.4917
Max Magnitude
? (A;A) (A;G) (G;G) 28
Rs348594
PubMed [PMID 17447842OA-icon.png]
Affy Probeset SNP_A-8391321
Affy Orientation same
On GW 5.0 0
Alleles A/B A/G
Ancestral G
Population EU
Allele A
Case Freq. 0.67
Control Freq. 0.6
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.36
Disease Crohn's disease (CD)


rs348594 is in linkage disequilibrium with a polymorphism that increases susceptibility to Crohn's disease 1.36 times for carriers of the A allele [PMID 17447842OA-icon.png]