rs11246602
From SNPedia
Orientation | minus |
Stabilized | plus |
Make rs11246602(C;C) |
Make rs11246602(C;T) |
Make rs11246602(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 11 |
Position | 54607190 |
is a | snp |
is | mentioned by |
dbSNP | rs11246602 |
dbSNP (classic) | rs11246602 |
ClinGen | rs11246602 |
ebi | rs11246602 |
HLI | rs11246602 |
Exac | rs11246602 |
Gnomad | rs11246602 |
Varsome | rs11246602 |
LitVar | rs11246602 |
Map | rs11246602 |
PheGenI | rs11246602 |
Biobank | rs11246602 |
1000 genomes | rs11246602 |
hgdp | rs11246602 |
ensembl | rs11246602 |
geneview | rs11246602 |
scholar | rs11246602 |
rs11246602 | |
pharmgkb | rs11246602 |
gwascentral | rs11246602 |
openSNP | rs11246602 |
23andMe | rs11246602 |
SNPshot | rs11246602 |
SNPdbe | rs11246602 |
MSV3d | rs11246602 |
GWAS Ctlg | rs11246602 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24097068] |
Trait | HDL cholesterol |
Title | Discovery and refinement of loci associated with lipid levels. |
Risk Allele | C |
P-val | 2E-10 |
Odds Ratio | .03 [NR] unit increase |