rs9266629
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9266629(C;C) |
Make rs9266629(C;T) |
Make rs9266629(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31379045 |
Gene | FGFR3P1 |
is a | snp |
is | mentioned by |
dbSNP | rs9266629 |
dbSNP (classic) | rs9266629 |
ClinGen | rs9266629 |
ebi | rs9266629 |
HLI | rs9266629 |
Exac | rs9266629 |
Gnomad | rs9266629 |
Varsome | rs9266629 |
LitVar | rs9266629 |
Map | rs9266629 |
PheGenI | rs9266629 |
Biobank | rs9266629 |
1000 genomes | rs9266629 |
hgdp | rs9266629 |
ensembl | rs9266629 |
geneview | rs9266629 |
scholar | rs9266629 |
rs9266629 | |
pharmgkb | rs9266629 |
gwascentral | rs9266629 |
openSNP | rs9266629 |
23andMe | rs9266629 |
SNPshot | rs9266629 |
SNPdbe | rs9266629 |
MSV3d | rs9266629 |
GWAS Ctlg | rs9266629 |
GMAF | 0.1543 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23144326] |
Trait | Chronic obstructive pulmonary disease-related biomarkers |
Title | Genome-Wide Association Analysis of Blood Biomarkers in Chronic Obstructive Pulmonary Disease. |
Risk Allele | C |
P-val | 4E-10 |
Odds Ratio | NR NR |
[PMID 19010793] Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
[PMID 19944404] Genomic dissection of population substructure of Han Chinese and its implication in association studies.