Have questions? Visit https://www.reddit.com/r/SNPedia

rs629301

From SNPedia

Orientationminus
Stabilizedminus
Make rs629301(A;A)
Make rs629301(A;C)
Make rs629301(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position109275684
GeneCELSR2
is asnp
is mentioned by
dbSNPrs629301
ebirs629301
HLIrs629301
Exacrs629301
Varsomers629301
Maprs629301
PheGenIrs629301
hapmaprs629301
1000 genomesrs629301
hgdprs629301
ensemblrs629301
gopubmedrs629301
geneviewrs629301
scholarrs629301
googlers629301
pharmgkbrs629301
gwascentralrs629301
openSNPrs629301
23andMers629301
23andMe allrs629301
SNP Nexus

SNPshotrs629301
SNPdbers629301
MSV3drs629301
GWAS Ctlgrs629301
GMAF0.2135
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20686565OA-icon.png]
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
OMIM613589
Desc
Variant
Relatedalso
[PMID 18262040OA-icon.png] LDL-cholesterol concentrations: a genome-wide association study.


[PMID 19913121OA-icon.png] Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.


[PMID 20502693OA-icon.png] Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.


[PMID 23092954OA-icon.png] SHAVE: shrinkage estimator measured for multiple visits increases power in GWAS of quantitative traits.


[PMID 23723249OA-icon.png] GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.

GWAS snp
PMID [PMID 24097068OA-icon.png]
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