rs7557067
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7557067(A;A) |
Make rs7557067(A;G) |
Make rs7557067(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 20985339 |
is a | snp |
is | mentioned by |
dbSNP | rs7557067 |
dbSNP (classic) | rs7557067 |
ClinGen | rs7557067 |
ebi | rs7557067 |
HLI | rs7557067 |
Exac | rs7557067 |
Gnomad | rs7557067 |
Varsome | rs7557067 |
LitVar | rs7557067 |
Map | rs7557067 |
PheGenI | rs7557067 |
Biobank | rs7557067 |
1000 genomes | rs7557067 |
hgdp | rs7557067 |
ensembl | rs7557067 |
geneview | rs7557067 |
scholar | rs7557067 |
rs7557067 | |
pharmgkb | rs7557067 |
gwascentral | rs7557067 |
openSNP | rs7557067 |
23andMe | rs7557067 |
SNPshot | rs7557067 |
SNPdbe | rs7557067 |
MSV3d | rs7557067 |
GWAS Ctlg | rs7557067 |
GMAF | 0.3476 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19060906] |
Trait | Triglycerides |
Title | Common variants at 30 loci contribute to polygenic dyslipidemia |
Risk Allele | G |
P-val | 9E-12 |
Odds Ratio | 0.08 [0.04-0.12] SD decrease |
[PMID 20160193] Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples.