rs796127
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs796127(A;A) |
Make rs796127(A;G) |
Make rs796127(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 31679801 |
is a | snp |
is | mentioned by |
dbSNP | rs796127 |
dbSNP (classic) | rs796127 |
ClinGen | rs796127 |
ebi | rs796127 |
HLI | rs796127 |
Exac | rs796127 |
Gnomad | rs796127 |
Varsome | rs796127 |
LitVar | rs796127 |
Map | rs796127 |
PheGenI | rs796127 |
Biobank | rs796127 |
1000 genomes | rs796127 |
hgdp | rs796127 |
ensembl | rs796127 |
geneview | rs796127 |
scholar | rs796127 |
rs796127 | |
pharmgkb | rs796127 |
gwascentral | rs796127 |
openSNP | rs796127 |
23andMe | rs796127 |
SNPshot | rs796127 |
SNPdbe | rs796127 |
MSV3d | rs796127 |
GWAS Ctlg | rs796127 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 3E-6 |
Odds Ratio | .09 [NR] unit decrease |