rs35136575
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs35136575(C;C) |
Make rs35136575(C;G) |
Make rs35136575(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 44935906 |
is a | snp |
is | mentioned by |
dbSNP | rs35136575 |
dbSNP (classic) | rs35136575 |
ClinGen | rs35136575 |
ebi | rs35136575 |
HLI | rs35136575 |
Exac | rs35136575 |
Gnomad | rs35136575 |
Varsome | rs35136575 |
LitVar | rs35136575 |
Map | rs35136575 |
PheGenI | rs35136575 |
Biobank | rs35136575 |
1000 genomes | rs35136575 |
hgdp | rs35136575 |
ensembl | rs35136575 |
geneview | rs35136575 |
scholar | rs35136575 |
rs35136575 | |
pharmgkb | rs35136575 |
gwascentral | rs35136575 |
openSNP | rs35136575 |
23andMe | rs35136575 |
SNPshot | rs35136575 |
SNPdbe | rs35136575 |
MSV3d | rs35136575 |
GWAS Ctlg | rs35136575 |
GMAF | 0.1699 |
Max Magnitude | 0 |
[PMID 18378515] 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 18801202] 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.