rs2954029

Orientation

plus

Stabilized

plus

Make rs2954029(A;A)

Make rs2954029(A;T)

Make rs2954029(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

125478730

is a	snp
is	mentioned by
dbSNP	rs2954029
dbSNP (classic)	rs2954029
ClinGen	rs2954029
ebi	rs2954029
HLI	rs2954029
Exac	rs2954029
Gnomad	rs2954029
Varsome	rs2954029
LitVar	rs2954029
Map	rs2954029
PheGenI	rs2954029
Biobank	rs2954029
1000 genomes	rs2954029
hgdp	rs2954029
ensembl	rs2954029
geneview	rs2954029
scholar	rs2954029
google	rs2954029
pharmgkb	rs2954029
gwascentral	rs2954029
openSNP	rs2954029
23andMe	rs2954029
SNPshot	rs2954029
SNPdbe	rs2954029
MSV3d	rs2954029
GWAS Ctlg	rs2954029

GMAF

0.4412

Max Magnitude

0

?	(A;A) (A;T) (T;T)	28

GWAS snp
PMID	[PMID 24097068]
Trait	HDL cholesterol
Title	Discovery and refinement of loci associated with lipid levels.
Risk Allele	T
P-val	3E-29
Odds Ratio	0.04 [NR] unit increase

GWAS snp
PMID	[PMID 24097068]
Trait	LDL cholesterol
Title	Discovery and refinement of loci associated with lipid levels.
Risk Allele	T
P-val	2E-50
Odds Ratio	0.056 [NR] unit decrease

GWAS snp
PMID	[PMID 24097068]
Trait	Triglycerides
Title	Discovery and refinement of loci associated with lipid levels.
Risk Allele	T
P-val	1E-107
Odds Ratio	0.076 [NR] mg/dL decrease

GWAS snp
PMID	[PMID 20864672]
Trait	Triglycerides
Title	Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Risk Allele	T
P-val	2E-11
Odds Ratio	0.04 [0.03-0.05] unit decrease

GWAS snp
PMID	[PMID 20686565]
Trait	HDL cholesterol
Title	Biological, clinical and population relevance of 95 loci for blood lipids.
Risk Allele	T
P-val	6E-19
Odds Ratio	0.61 [0.47-0.75] mg/dL increase

GWAS snp
PMID	[PMID 20686565]
Trait	LDL cholesterol
Title	Biological, clinical and population relevance of 95 loci for blood lipids.
Risk Allele	A
P-val	3E-29
Odds Ratio	1.84 [1.51-2.17] mg/dL decrease

GWAS snp
PMID	[PMID 20686565]
Trait	Triglycerides
Title	Biological, clinical and population relevance of 95 loci for blood lipids.
Risk Allele	T
P-val	3E-55
Odds Ratio	5.64 [4.88-6.4] mg/dL decrease

GWAS snp
PMID	[PMID 20139978]
Trait	Triglycerides
Title	Genome-wide association study of hematological and biochemical traits in a Japanese population.
Risk Allele	T
P-val	3E-7
Odds Ratio	0.076 [0.047-0.105] unit decrease

GWAS snp
PMID	[PMID 19060906]
Trait	Triglycerides
Title	Common variants at 30 loci contribute to polygenic dyslipidemia
Risk Allele	T
P-val	3E-19
Odds Ratio	0.11 [0.07-0.15] SD decrease

GWAS snp
PMID	[PMID 19060906]
Trait	Triglycerides
Title	Common variants at 30 loci contribute to polygenic dyslipidemia.
Risk Allele	T
P-val	3E-19
Odds Ratio	0.11 [0.07-0.15] s.d. decrease

[PMID 24922540] Genetic Determinants of Long-Term Changes in Blood Lipid Concentrations: 10-Year Follow-Up of the GLACIER Study

[PMID 23832694] Common genetic variants associated with lipid profiles in a Chinese pediatric population.

[PMID 23202125] Large-scale association analysis identifies new risk loci for coronary artery disease.

[PMID 21071687] TRIB1 and GCKR polymorphisms, lipid levels, and risk of ischemic heart disease in the general population.

[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.

[PMID 19656773] A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia.