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rs9637876

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9637876(C;T)
Make rs9637876(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position150847863
GeneIRGM
is asnp
is mentioned by
dbSNPrs9637876
ebirs9637876
HLIrs9637876
Exacrs9637876
Varsomers9637876
Maprs9637876
PheGenIrs9637876
hapmaprs9637876
1000 genomesrs9637876
hgdprs9637876
ensemblrs9637876
gopubmedrs9637876
geneviewrs9637876
scholarrs9637876
googlers9637876
pharmgkbrs9637876
gwascentralrs9637876
openSNPrs9637876
23andMers9637876
23andMe allrs9637876
SNP Nexus

SNPshotrs9637876
SNPdbers9637876
MSV3drs9637876
GWAS Ctlgrs9637876
GMAF0.2388
Max Magnitude0
OMIM608212
DescIMMUNITY-RELATED GTPase FAMILY, M; IRGM
Variant
Relatedalso
OMIM607948
Desc
Variant
Relatedalso
[PMID 19750224OA-icon.png] Autophagy gene variant IRGM -261T contributes to protection from tuberculosis caused by Mycobacterium tuberculosis but not by M. africanum strains.


[PMID 20106866OA-icon.png] Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.