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

rs4765127

From SNPedia

Orientationplus
Stabilizedplus
Make rs4765127(G;G)
Make rs4765127(G;T)
Make rs4765127(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position123975620
GeneZNF664, ZNF664-FAM101A
is asnp
is mentioned by
dbSNPrs4765127
ebirs4765127
HLIrs4765127
Exacrs4765127
Varsomers4765127
Maprs4765127
PheGenIrs4765127
hapmaprs4765127
1000 genomesrs4765127
hgdprs4765127
ensemblrs4765127
gopubmedrs4765127
geneviewrs4765127
scholarrs4765127
googlers4765127
pharmgkbrs4765127
gwascentralrs4765127
openSNPrs4765127
23andMers4765127
23andMe allrs4765127
SNP Nexus

SNPshotrs4765127
SNPdbers4765127
MSV3drs4765127
GWAS Ctlgrs4765127
GMAF0.2842
Max Magnitude
? (G;G) (G;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 1E-8
Odds Ratio 2.4200 None
GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait HDL cholesterol
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele T
P-val 8E-10
Odds Ratio .03 [NR] unit increase