rs7671266
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7671266(C;C) |
Make rs7671266(C;T) |
Make rs7671266(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 10054752 |
is a | snp |
is | mentioned by |
dbSNP | rs7671266 |
dbSNP (classic) | rs7671266 |
ClinGen | rs7671266 |
ebi | rs7671266 |
HLI | rs7671266 |
Exac | rs7671266 |
Gnomad | rs7671266 |
Varsome | rs7671266 |
LitVar | rs7671266 |
Map | rs7671266 |
PheGenI | rs7671266 |
Biobank | rs7671266 |
1000 genomes | rs7671266 |
hgdp | rs7671266 |
ensembl | rs7671266 |
geneview | rs7671266 |
scholar | rs7671266 |
rs7671266 | |
pharmgkb | rs7671266 |
gwascentral | rs7671266 |
openSNP | rs7671266 |
23andMe | rs7671266 |
SNPshot | rs7671266 |
SNPdbe | rs7671266 |
MSV3d | rs7671266 |
GWAS Ctlg | rs7671266 |
GMAF | 0.2153 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21943158![]() |
Trait | |
Title | Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. |
Risk Allele | T |
P-val | 9E-71 |
Odds Ratio | 0.3050 [0.27-0.34] umol/l decrease |