rs10091374
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10091374(A;A) |
Make rs10091374(A;T) |
Make rs10091374(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 70474669 |
Gene | LOC101926892 |
is a | snp |
is | mentioned by |
dbSNP | rs10091374 |
dbSNP (classic) | rs10091374 |
ClinGen | rs10091374 |
ebi | rs10091374 |
HLI | rs10091374 |
Exac | rs10091374 |
Gnomad | rs10091374 |
Varsome | rs10091374 |
LitVar | rs10091374 |
Map | rs10091374 |
PheGenI | rs10091374 |
Biobank | rs10091374 |
1000 genomes | rs10091374 |
hgdp | rs10091374 |
ensembl | rs10091374 |
geneview | rs10091374 |
scholar | rs10091374 |
rs10091374 | |
pharmgkb | rs10091374 |
gwascentral | rs10091374 |
openSNP | rs10091374 |
23andMe | rs10091374 |
SNPshot | rs10091374 |
SNPdbe | rs10091374 |
MSV3d | rs10091374 |
GWAS Ctlg | rs10091374 |
GMAF | 0.4871 |
Max Magnitude | 0 |
? | (A;A) (A;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 | A |
P-val | 9E-9 |
Odds Ratio | .04 [0.027-0.059] ug/L decrease |