rs2217332
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2217332(C;C) |
Make rs2217332(C;T) |
Make rs2217332(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 16 |
Position | 56935236 |
Gene | HERPUD1 |
is a | snp |
is | mentioned by |
dbSNP | rs2217332 |
dbSNP (classic) | rs2217332 |
ClinGen | rs2217332 |
ebi | rs2217332 |
HLI | rs2217332 |
Exac | rs2217332 |
Gnomad | rs2217332 |
Varsome | rs2217332 |
LitVar | rs2217332 |
Map | rs2217332 |
PheGenI | rs2217332 |
Biobank | rs2217332 |
1000 genomes | rs2217332 |
hgdp | rs2217332 |
ensembl | rs2217332 |
geneview | rs2217332 |
scholar | rs2217332 |
rs2217332 | |
pharmgkb | rs2217332 |
gwascentral | rs2217332 |
openSNP | rs2217332 |
23andMe | rs2217332 |
SNPshot | rs2217332 |
SNPdbe | rs2217332 |
MSV3d | rs2217332 |
GWAS Ctlg | rs2217332 |
GMAF | 0.1166 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20694148![]() |
Trait | |
Title | A genome-wide association study of the metabolic syndrome in Indian Asian men |
Risk Allele | |
P-val | 0.000003 |
Odds Ratio | None None |
[PMID 20031564] Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study.
[PMID 26823705] Evidence of a novel gene HERPUD1 in polypoidal choroidal vasculopathy.