rs72553867
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs72553867(A;A) |
Make rs72553867(A;C) |
Make rs72553867(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 150848404 |
Gene | IRGM |
is a | snp |
is | mentioned by |
dbSNP | rs72553867 |
dbSNP (classic) | rs72553867 |
ClinGen | rs72553867 |
ebi | rs72553867 |
HLI | rs72553867 |
Exac | rs72553867 |
Gnomad | rs72553867 |
Varsome | rs72553867 |
LitVar | rs72553867 |
Map | rs72553867 |
PheGenI | rs72553867 |
Biobank | rs72553867 |
1000 genomes | rs72553867 |
hgdp | rs72553867 |
ensembl | rs72553867 |
geneview | rs72553867 |
scholar | rs72553867 |
rs72553867 | |
pharmgkb | rs72553867 |
gwascentral | rs72553867 |
openSNP | rs72553867 |
23andMe | rs72553867 |
SNPshot | rs72553867 |
SNPdbe | rs72553867 |
MSV3d | rs72553867 |
GWAS Ctlg | rs72553867 |
GMAF | 0.07163 |
Max Magnitude | 0 |
[PMID 22508677] Associations between genetic variants in the IRGM gene and inflammatory bowel diseases in the Korean population [PMID 19750224] Autophagy gene variant IRGM -261T contributes to protection from tuberculosis caused by Mycobacterium tuberculosis but not by M. africanum strains.
[PMID 31844038] Polymorphisms of the TNF Gene and Three Susceptibility Loci Are Associated with Crohn's Disease and Perianal Fistula Crohn's Disease: A Study among the Han Population from South China.