rs9637876
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs9637876(C;T) |
Make rs9637876(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 150847863 |
Gene | IRGM |
is a | snp |
is | mentioned by |
dbSNP | rs9637876 |
dbSNP (classic) | rs9637876 |
ClinGen | rs9637876 |
ebi | rs9637876 |
HLI | rs9637876 |
Exac | rs9637876 |
Gnomad | rs9637876 |
Varsome | rs9637876 |
LitVar | rs9637876 |
Map | rs9637876 |
PheGenI | rs9637876 |
Biobank | rs9637876 |
1000 genomes | rs9637876 |
hgdp | rs9637876 |
ensembl | rs9637876 |
geneview | rs9637876 |
scholar | rs9637876 |
rs9637876 | |
pharmgkb | rs9637876 |
gwascentral | rs9637876 |
openSNP | rs9637876 |
23andMe | rs9637876 |
SNPshot | rs9637876 |
SNPdbe | rs9637876 |
MSV3d | rs9637876 |
GWAS Ctlg | rs9637876 |
GMAF | 0.2388 |
Max Magnitude | 0 |
[PMID 19750224] Autophagy gene variant IRGM -261T contributes to protection from tuberculosis caused by Mycobacterium tuberculosis but not by M. africanum strains.
[PMID 20106866] Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.
[PMID 30335469] Crohn's disease IRGM risk alleles are associated with altered gene expression in human tissues.