rs11886999
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11886999(C;C) |
Make rs11886999(C;T) |
Make rs11886999(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 96176055 |
is a | snp |
is | mentioned by |
dbSNP | rs11886999 |
dbSNP (classic) | rs11886999 |
ClinGen | rs11886999 |
ebi | rs11886999 |
HLI | rs11886999 |
Exac | rs11886999 |
Gnomad | rs11886999 |
Varsome | rs11886999 |
LitVar | rs11886999 |
Map | rs11886999 |
PheGenI | rs11886999 |
Biobank | rs11886999 |
1000 genomes | rs11886999 |
hgdp | rs11886999 |
ensembl | rs11886999 |
geneview | rs11886999 |
scholar | rs11886999 |
rs11886999 | |
pharmgkb | rs11886999 |
gwascentral | rs11886999 |
openSNP | rs11886999 |
23andMe | rs11886999 |
SNPshot | rs11886999 |
SNPdbe | rs11886999 |
MSV3d | rs11886999 |
GWAS Ctlg | rs11886999 |
GMAF | 0.2438 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23247143] |
Trait | Cardiac Troponin-T levels |
Title | Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European americans and blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies. |
Risk Allele | T |
P-val | 8E-6 |
Odds Ratio | .04 [0.02-0.06] ug/L increase |