rs17596685
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17596685(C;C) |
Make rs17596685(C;T) |
Make rs17596685(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 13 |
Position | 42543065 |
is a | snp |
is | mentioned by |
dbSNP | rs17596685 |
dbSNP (classic) | rs17596685 |
ClinGen | rs17596685 |
ebi | rs17596685 |
HLI | rs17596685 |
Exac | rs17596685 |
Gnomad | rs17596685 |
Varsome | rs17596685 |
LitVar | rs17596685 |
Map | rs17596685 |
PheGenI | rs17596685 |
Biobank | rs17596685 |
1000 genomes | rs17596685 |
hgdp | rs17596685 |
ensembl | rs17596685 |
geneview | rs17596685 |
scholar | rs17596685 |
rs17596685 | |
pharmgkb | rs17596685 |
gwascentral | rs17596685 |
openSNP | rs17596685 |
23andMe | rs17596685 |
SNPshot | rs17596685 |
SNPdbe | rs17596685 |
MSV3d | rs17596685 |
GWAS Ctlg | rs17596685 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24763700] |
Trait | C-reactive protein levels |
Title | New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. |
Risk Allele | T |
P-val | 4E-6 |
Odds Ratio | .09 [NR] unit decrease |