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rs2371685

From SNPedia

Orientationplus
Stabilizedplus
Make rs2371685(A;A)
Make rs2371685(A;T)
Make rs2371685(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position40392124
is asnp
is mentioned by
dbSNPrs2371685
ebirs2371685
HLIrs2371685
Exacrs2371685
Varsomers2371685
Maprs2371685
PheGenIrs2371685
hapmaprs2371685
1000 genomesrs2371685
hgdprs2371685
ensemblrs2371685
gopubmedrs2371685
geneviewrs2371685
scholarrs2371685
googlers2371685
pharmgkbrs2371685
gwascentralrs2371685
openSNPrs2371685
23andMers2371685
23andMe allrs2371685
SNP Nexus

SNPshotrs2371685
SNPdbers2371685
MSV3drs2371685
GWAS Ctlgrs2371685
GMAF0.1097
Max Magnitude
? (A;A) (A;T) (T;T) 28
Rs2371685
PubMed [PMID 17447842OA-icon.png]
Affy Probeset SNP_A-4264860
Affy Orientation same
On GW 5.0 1
Alleles A/B A/T
Ancestral A
Population EU
Allele T
Case Freq. 0.19
Control Freq. 0.13
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.56
Disease Crohn's disease (CD)


rs2371685 is in linkage disequilibrium with a polymorphism that increases susceptibility to Crohn's disease 1.56 times for carriers of the T allele [PMID 17447842OA-icon.png]

Neighborrs4613763
Distance502
[PMID 17903294OA-icon.png] Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.