rs1985317
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1985317(A;A) |
Make rs1985317(A;G) |
Make rs1985317(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 117530056 |
is a | snp |
is | mentioned by |
dbSNP | rs1985317 |
dbSNP (classic) | rs1985317 |
ClinGen | rs1985317 |
ebi | rs1985317 |
HLI | rs1985317 |
Exac | rs1985317 |
Gnomad | rs1985317 |
Varsome | rs1985317 |
LitVar | rs1985317 |
Map | rs1985317 |
PheGenI | rs1985317 |
Biobank | rs1985317 |
1000 genomes | rs1985317 |
hgdp | rs1985317 |
ensembl | rs1985317 |
geneview | rs1985317 |
scholar | rs1985317 |
rs1985317 | |
pharmgkb | rs1985317 |
gwascentral | rs1985317 |
openSNP | rs1985317 |
23andMe | rs1985317 |
SNPshot | rs1985317 |
SNPdbe | rs1985317 |
MSV3d | rs1985317 |
GWAS Ctlg | rs1985317 |
GMAF | 0.4004 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23509962] |
Trait | Venous thromboembolism (gene x gene interaction) |
Title | A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. |
Risk Allele | |
P-val | 1E-9 |
Odds Ratio | 1.52 [NR] |