rs111521887
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs111521887(C;C) |
Make rs111521887(C;G) |
Make rs111521887(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 1291476 |
Gene | TOLLIP |
is a | snp |
is | mentioned by |
dbSNP | rs111521887 |
dbSNP (classic) | rs111521887 |
ClinGen | rs111521887 |
ebi | rs111521887 |
HLI | rs111521887 |
Exac | rs111521887 |
Gnomad | rs111521887 |
Varsome | rs111521887 |
LitVar | rs111521887 |
Map | rs111521887 |
PheGenI | rs111521887 |
Biobank | rs111521887 |
1000 genomes | rs111521887 |
hgdp | rs111521887 |
ensembl | rs111521887 |
geneview | rs111521887 |
scholar | rs111521887 |
rs111521887 | |
pharmgkb | rs111521887 |
gwascentral | rs111521887 |
openSNP | rs111521887 |
23andMe | rs111521887 |
SNPshot | rs111521887 |
SNPdbe | rs111521887 |
MSV3d | rs111521887 |
GWAS Ctlg | rs111521887 |
GMAF | 0.08448 |
Max Magnitude | 0 |
[PMID 24429156] Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study