rs9898
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9898(C;C) |
Make rs9898(C;T) |
Make rs9898(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 186672838 |
Gene | HRG, LOC105374258 |
is a | snp |
is | mentioned by |
dbSNP | rs9898 |
dbSNP (classic) | rs9898 |
ClinGen | rs9898 |
ebi | rs9898 |
HLI | rs9898 |
Exac | rs9898 |
Gnomad | rs9898 |
Varsome | rs9898 |
LitVar | rs9898 |
Map | rs9898 |
PheGenI | rs9898 |
Biobank | rs9898 |
1000 genomes | rs9898 |
hgdp | rs9898 |
ensembl | rs9898 |
geneview | rs9898 |
scholar | rs9898 |
rs9898 | |
pharmgkb | rs9898 |
gwascentral | rs9898 |
openSNP | rs9898 |
23andMe | rs9898 |
SNPshot | rs9898 |
SNPdbe | rs9898 |
MSV3d | rs9898 |
GWAS Ctlg | rs9898 |
GMAF | 0.4633 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20303064] |
Trait | Activated partial thromboplastin time |
Title | Common Variants of Large Effect in F12, KNG1, and HRG Are Associated with Activated Partial Thromboplastin Time |
Risk Allele | T |
P-val | 1E-11 |
Odds Ratio | 0.26 [0.19-0.33] unit increase |
[PMID 21270443] KNG1 Ile581Thr and susceptibility to venous thrombosis.
GWAS snp | |
---|---|
PMID | [PMID 22703881] |
Trait | |
Title | Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease. |
Risk Allele | C |
P-val | 1E-111 |
Odds Ratio | 1.0000 None |