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rs2096525

From SNPedia

Orientationplus
Stabilizedplus
Make rs2096525(C;C)
Make rs2096525(C;T)
Make rs2096525(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position23894632
GeneLOC284889, MIF
is asnp
is mentioned by
dbSNPrs2096525
ebirs2096525
HLIrs2096525
Exacrs2096525
Varsomers2096525
Maprs2096525
PheGenIrs2096525
hapmaprs2096525
1000 genomesrs2096525
hgdprs2096525
ensemblrs2096525
gopubmedrs2096525
geneviewrs2096525
scholarrs2096525
googlers2096525
pharmgkbrs2096525
gwascentralrs2096525
openSNPrs2096525
23andMers2096525
23andMe allrs2096525
SNP Nexus

SNPshotrs2096525
SNPdbers2096525
MSV3drs2096525
GWAS Ctlgrs2096525
GMAF0.2126
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 24194192] MIF gene polymorphisms confer susceptibility to Vogt-Koyanagi-Harada syndrome in a Han Chinese population [PMID 22939113] Association of macrophage migration inhibitory factor gene polymorphisms with Behcet's disease in a Han Chinese population. [PMID 26825917] MIF Gene Polymorphism rs755622 Is Associated With Coronary Artery Disease and Severity of Coronary Lesions in a Chinese Kazakh Population: A Case-Control Study.