rs17690703
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17690703(C;C) |
Make rs17690703(C;T) |
Make rs17690703(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 45847931 |
Gene | MAPT-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs17690703 |
dbSNP (classic) | rs17690703 |
ClinGen | rs17690703 |
ebi | rs17690703 |
HLI | rs17690703 |
Exac | rs17690703 |
Gnomad | rs17690703 |
Varsome | rs17690703 |
LitVar | rs17690703 |
Map | rs17690703 |
PheGenI | rs17690703 |
Biobank | rs17690703 |
1000 genomes | rs17690703 |
hgdp | rs17690703 |
ensembl | rs17690703 |
geneview | rs17690703 |
scholar | rs17690703 |
rs17690703 | |
pharmgkb | rs17690703 |
gwascentral | rs17690703 |
openSNP | rs17690703 |
23andMe | rs17690703 |
SNPshot | rs17690703 |
SNPdbe | rs17690703 |
MSV3d | rs17690703 |
GWAS Ctlg | rs17690703 |
GMAF | 0.1543 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24429156] |
Trait | Idiopathic pulmonary fibrosis |
Title | Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study |
Risk Allele | |
P-val | |
Odds Ratio |