rs629301
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs629301(A;A) |
Make rs629301(A;C) |
Make rs629301(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 109275684 |
Gene | CELSR2 |
is a | snp |
is | mentioned by |
dbSNP | rs629301 |
dbSNP (classic) | rs629301 |
ClinGen | rs629301 |
ebi | rs629301 |
HLI | rs629301 |
Exac | rs629301 |
Gnomad | rs629301 |
Varsome | rs629301 |
LitVar | rs629301 |
Map | rs629301 |
PheGenI | rs629301 |
Biobank | rs629301 |
1000 genomes | rs629301 |
hgdp | rs629301 |
ensembl | rs629301 |
geneview | rs629301 |
scholar | rs629301 |
rs629301 | |
pharmgkb | rs629301 |
gwascentral | rs629301 |
openSNP | rs629301 |
23andMe | rs629301 |
SNPshot | rs629301 |
SNPdbe | rs629301 |
MSV3d | rs629301 |
GWAS Ctlg | rs629301 |
GMAF | 0.2135 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20686565![]() |
Trait | |
Title | Biological, clinical and population relevance of 95 loci for blood lipids |
Risk Allele | G |
P-val | 0 |
Odds Ratio | 5.65 [NR] unit decrease |
[PMID 18262040] LDL-cholesterol concentrations: a genome-wide association study.
[PMID 19913121] Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
[PMID 20502693] Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.
[PMID 23092954] SHAVE: shrinkage estimator measured for multiple visits increases power in GWAS of quantitative traits.
[PMID 23723249] GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.
GWAS snp | |
---|---|
PMID | [PMID 24097068![]() |
Trait | Cholesterol, total |
Title | Discovery and refinement of loci associated with lipid levels. |
Risk Allele | G |
P-val | 2E-170 |
Odds Ratio | .13 [NR] unit decrease |