rs1154988
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1154988(A;A) |
Make rs1154988(A;T) |
Make rs1154988(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 3 |
Position | 136206349 |
is a | snp |
is | mentioned by |
dbSNP | rs1154988 |
dbSNP (classic) | rs1154988 |
ClinGen | rs1154988 |
ebi | rs1154988 |
HLI | rs1154988 |
Exac | rs1154988 |
Gnomad | rs1154988 |
Varsome | rs1154988 |
LitVar | rs1154988 |
Map | rs1154988 |
PheGenI | rs1154988 |
Biobank | rs1154988 |
1000 genomes | rs1154988 |
hgdp | rs1154988 |
ensembl | rs1154988 |
geneview | rs1154988 |
scholar | rs1154988 |
rs1154988 | |
pharmgkb | rs1154988 |
gwascentral | rs1154988 |
openSNP | rs1154988 |
23andMe | rs1154988 |
SNPshot | rs1154988 |
SNPdbe | rs1154988 |
MSV3d | rs1154988 |
GWAS Ctlg | rs1154988 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23969696] |
Trait | Fibrinogen |
Title | Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. |
Risk Allele | A |
P-val | 1E-16 |
Odds Ratio | .01 [0.008-0.012] unit decrease |