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rs4775065

From SNPedia

Orientationplus
Stabilizedplus
Make rs4775065(A;A)
Make rs4775065(A;G)
Make rs4775065(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position58509744
GeneLIPC
is asnp
is mentioned by
dbSNPrs4775065
ebirs4775065
HLIrs4775065
Exacrs4775065
Varsomers4775065
Maprs4775065
PheGenIrs4775065
hapmaprs4775065
1000 genomesrs4775065
hgdprs4775065
ensemblrs4775065
gopubmedrs4775065
geneviewrs4775065
scholarrs4775065
googlers4775065
pharmgkbrs4775065
gwascentralrs4775065
openSNPrs4775065
23andMers4775065
23andMe allrs4775065
SNP Nexus

SNPshotrs4775065
SNPdbers4775065
MSV3drs4775065
GWAS Ctlgrs4775065
GMAF0.2851
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20855565OA-icon.png] Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease


[PMID 19101670OA-icon.png] LIPC variants in the promoter and intron 1 modify HDL-C levels in a sex-specific fashion.