rs2142672
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2142672(C;C) |
Make rs2142672(C;T) |
Make rs2142672(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 16196963 |
is a | snp |
is | mentioned by |
dbSNP | rs2142672 |
dbSNP (classic) | rs2142672 |
ClinGen | rs2142672 |
ebi | rs2142672 |
HLI | rs2142672 |
Exac | rs2142672 |
Gnomad | rs2142672 |
Varsome | rs2142672 |
LitVar | rs2142672 |
Map | rs2142672 |
PheGenI | rs2142672 |
Biobank | rs2142672 |
1000 genomes | rs2142672 |
hgdp | rs2142672 |
ensembl | rs2142672 |
geneview | rs2142672 |
scholar | rs2142672 |
rs2142672 | |
pharmgkb | rs2142672 |
gwascentral | rs2142672 |
openSNP | rs2142672 |
23andMe | rs2142672 |
SNPshot | rs2142672 |
SNPdbe | rs2142672 |
MSV3d | rs2142672 |
GWAS Ctlg | rs2142672 |
GMAF | 0.4844 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20864672] |
Trait | |
Title | Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease |
Risk Allele | C |
P-val | 2E-8 |
Odds Ratio | 0.01 [0.007-0.015] unit increase |