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rs7941030

From SNPedia

Orientationplus
Stabilizedplus
Make rs7941030(C;C)
Make rs7941030(C;T)
Make rs7941030(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position122651667
is asnp
is mentioned by
dbSNPrs7941030
ebirs7941030
HLIrs7941030
Exacrs7941030
Varsomers7941030
Maprs7941030
PheGenIrs7941030
hapmaprs7941030
1000 genomesrs7941030
hgdprs7941030
ensemblrs7941030
gopubmedrs7941030
geneviewrs7941030
scholarrs7941030
googlers7941030
pharmgkbrs7941030
gwascentralrs7941030
openSNPrs7941030
23andMers7941030
23andMe allrs7941030
SNP Nexus

SNPshotrs7941030
SNPdbers7941030
MSV3drs7941030
GWAS Ctlgrs7941030
GMAF0.3779
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20686565OA-icon.png]
Trait
Title Biological, clinical and population relevance of 95 loci for blood lipids.
Risk Allele C
P-val 2E-10
Odds Ratio 0.9700 None
GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait Cholesterol, total
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele C
P-val 2E-14
Odds Ratio .03 [NR] unit increase