rs10007052
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10007052(A;A) |
Make rs10007052(A;C) |
Make rs10007052(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 141084419 |
Gene | RNF150 |
is a | snp |
is | mentioned by |
dbSNP | rs10007052 |
dbSNP (classic) | rs10007052 |
ClinGen | rs10007052 |
ebi | rs10007052 |
HLI | rs10007052 |
Exac | rs10007052 |
Gnomad | rs10007052 |
Varsome | rs10007052 |
LitVar | rs10007052 |
Map | rs10007052 |
PheGenI | rs10007052 |
Biobank | rs10007052 |
1000 genomes | rs10007052 |
hgdp | rs10007052 |
ensembl | rs10007052 |
geneview | rs10007052 |
scholar | rs10007052 |
rs10007052 | |
pharmgkb | rs10007052 |
gwascentral | rs10007052 |
openSNP | rs10007052 |
23andMe | rs10007052 |
SNPshot | rs10007052 |
SNPdbe | rs10007052 |
MSV3d | rs10007052 |
GWAS Ctlg | rs10007052 |
GMAF | 0.4219 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | A |
P-val | 1E-7 |
Odds Ratio | NR NR |