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rs35136575

From SNPedia

Orientationplus
Stabilizedplus
Make rs35136575(C;C)
Make rs35136575(C;G)
Make rs35136575(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44935906
is asnp
is mentioned by
dbSNPrs35136575
ebirs35136575
HLIrs35136575
Exacrs35136575
Varsomers35136575
Maprs35136575
PheGenIrs35136575
hapmaprs35136575
1000 genomesrs35136575
hgdprs35136575
ensemblrs35136575
gopubmedrs35136575
geneviewrs35136575
scholarrs35136575
googlers35136575
pharmgkbrs35136575
gwascentralrs35136575
openSNPrs35136575
23andMers35136575
23andMe allrs35136575
SNP Nexus

SNPshotrs35136575
SNPdbers35136575
MSV3drs35136575
GWAS Ctlgrs35136575
GMAF0.1699
Max Magnitude
[PMID 18378515OA-icon.png] Lower plasma LDL-C was observed with the rare allele. Plasma apoE level was strongly associated with HCR-2 variant genotype in all three GENOA samples (p</=0.002), indicating an effect on apoE concentration.

[PMID 18801202OA-icon.png] Genetic studies on the APOA1-C3-A5 gene cluster in Asian Indians with premature coronary artery disease.


[PMID 22715478] Genotypes associated with lipid metabolism contribute to differences in serum lipid profile of GH-deficient adults before and after GH replacement therapy.