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rs605066

From SNPedia

Orientationplus
Stabilizedplus
Make rs605066(C;C)
Make rs605066(C;T)
Make rs605066(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position139508529
is asnp
is mentioned by
dbSNPrs605066
ebirs605066
HLIrs605066
Exacrs605066
Varsomers605066
Maprs605066
PheGenIrs605066
hapmaprs605066
1000 genomesrs605066
hgdprs605066
ensemblrs605066
gopubmedrs605066
geneviewrs605066
scholarrs605066
googlers605066
pharmgkbrs605066
gwascentralrs605066
openSNPrs605066
23andMers605066
23andMe allrs605066
SNP Nexus

SNPshotrs605066
SNPdbers605066
MSV3drs605066
GWAS Ctlgrs605066
GMAF0.461
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 3E-8
Odds Ratio 0.3900 None
GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait HDL cholesterol
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele C
P-val 3E-8
Odds Ratio .03 [NR] unit decrease