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rs9686661

From SNPedia

Orientationplus
Stabilizedplus
Make rs9686661(C;C)
Make rs9686661(C;T)
Make rs9686661(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position56565959
GeneLOC101928448
is asnp
is mentioned by
dbSNPrs9686661
ebirs9686661
HLIrs9686661
Exacrs9686661
Varsomers9686661
Maprs9686661
PheGenIrs9686661
hapmaprs9686661
1000 genomesrs9686661
hgdprs9686661
ensemblrs9686661
gopubmedrs9686661
geneviewrs9686661
scholarrs9686661
googlers9686661
pharmgkbrs9686661
gwascentralrs9686661
openSNPrs9686661
23andMers9686661
23andMe allrs9686661
SNP Nexus

SNPshotrs9686661
SNPdbers9686661
MSV3drs9686661
GWAS Ctlgrs9686661
GMAF0.1869
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 T
P-val 1E-10
Odds Ratio 2.5700 None
GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait Triglycerides
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele T
P-val 3E-16
Odds Ratio .04 [NR] mg/dL increase