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rs4129767

From SNPedia

Orientationminus
Stabilizedminus
Make rs4129767(C;C)
Make rs4129767(C;T)
Make rs4129767(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position78407903
GenePGS1
is asnp
is mentioned by
dbSNPrs4129767
ebirs4129767
HLIrs4129767
Exacrs4129767
Varsomers4129767
Maprs4129767
PheGenIrs4129767
hapmaprs4129767
1000 genomesrs4129767
hgdprs4129767
ensemblrs4129767
gopubmedrs4129767
geneviewrs4129767
scholarrs4129767
googlers4129767
pharmgkbrs4129767
gwascentralrs4129767
openSNPrs4129767
23andMers4129767
23andMe allrs4129767
SNP Nexus

SNPshotrs4129767
SNPdbers4129767
MSV3drs4129767
GWAS Ctlgrs4129767
GMAF0.4449
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 G
P-val 5E-9
Odds Ratio 0.4000 None
GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait HDL cholesterol
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele G
P-val 2E-11
Odds Ratio .02 [NR] unit decrease