rs12602901
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12602901(C;C) |
Make rs12602901(C;G) |
Make rs12602901(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 4921330 |
is a | snp |
is | mentioned by |
dbSNP | rs12602901 |
dbSNP (classic) | rs12602901 |
ClinGen | rs12602901 |
ebi | rs12602901 |
HLI | rs12602901 |
Exac | rs12602901 |
Gnomad | rs12602901 |
Varsome | rs12602901 |
LitVar | rs12602901 |
Map | rs12602901 |
PheGenI | rs12602901 |
Biobank | rs12602901 |
1000 genomes | rs12602901 |
hgdp | rs12602901 |
ensembl | rs12602901 |
geneview | rs12602901 |
scholar | rs12602901 |
rs12602901 | |
pharmgkb | rs12602901 |
gwascentral | rs12602901 |
openSNP | rs12602901 |
23andMe | rs12602901 |
SNPshot | rs12602901 |
SNPdbe | rs12602901 |
MSV3d | rs12602901 |
GWAS Ctlg | rs12602901 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24816252] |
Trait | Blood metabolite levels |
Title | An atlas of genetic influences on human blood metabolites. |
Risk Allele | C |
P-val | 1E-26 |
Odds Ratio | .04 [0.031-0.043] unit decrease |