rs2081687
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2081687(A;A) |
Make rs2081687(A;G) |
Make rs2081687(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 58476006 |
is a | snp |
is | mentioned by |
dbSNP | rs2081687 |
dbSNP (classic) | rs2081687 |
ClinGen | rs2081687 |
ebi | rs2081687 |
HLI | rs2081687 |
Exac | rs2081687 |
Gnomad | rs2081687 |
Varsome | rs2081687 |
LitVar | rs2081687 |
Map | rs2081687 |
PheGenI | rs2081687 |
Biobank | rs2081687 |
1000 genomes | rs2081687 |
hgdp | rs2081687 |
ensembl | rs2081687 |
geneview | rs2081687 |
scholar | rs2081687 |
rs2081687 | |
pharmgkb | rs2081687 |
gwascentral | rs2081687 |
openSNP | rs2081687 |
23andMe | rs2081687 |
SNPshot | rs2081687 |
SNPdbe | rs2081687 |
MSV3d | rs2081687 |
GWAS Ctlg | rs2081687 |
GMAF | 0.2645 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20686565![]() |
Trait | |
Title | Biological, clinical and population relevance of 95 loci for blood lipids. |
Risk Allele | A |
P-val | 9E-13 |
Odds Ratio | 1.2600 None |
GWAS snp | |
---|---|
PMID | [PMID 24097068![]() |
Trait | Cholesterol, total |
Title | Discovery and refinement of loci associated with lipid levels. |
Risk Allele | T |
P-val | 9E-12 |
Odds Ratio | .04 [NR] unit increase |