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rs599838

From SNPedia

Orientationplus
Stabilizedplus
Make rs599838(C;C)
Make rs599838(C;T)
Make rs599838(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position9788351
is asnp
is mentioned by
dbSNPrs599838
ebirs599838
HLIrs599838
Exacrs599838
Varsomers599838
Maprs599838
PheGenIrs599838
hapmaprs599838
1000 genomesrs599838
hgdprs599838
ensemblrs599838
gopubmedrs599838
geneviewrs599838
scholarrs599838
googlers599838
pharmgkbrs599838
gwascentralrs599838
openSNPrs599838
23andMers599838
23andMe allrs599838
SNP Nexus

SNPshotrs599838
SNPdbers599838
MSV3drs599838
GWAS Ctlgrs599838
Max Magnitude

[PMID 23098650] Impact of variants within seven candidate genes on statin treatment efficacy [PMID 18193044OA-icon.png] Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.


[PMID 19060911OA-icon.png] Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.