rs3917615
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3917615(A;A) |
Make rs3917615(A;G) |
Make rs3917615(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 94536434 |
Gene | F3 |
is a | snp |
is | mentioned by |
dbSNP | rs3917615 |
dbSNP (classic) | rs3917615 |
ClinGen | rs3917615 |
ebi | rs3917615 |
HLI | rs3917615 |
Exac | rs3917615 |
Gnomad | rs3917615 |
Varsome | rs3917615 |
LitVar | rs3917615 |
Map | rs3917615 |
PheGenI | rs3917615 |
Biobank | rs3917615 |
1000 genomes | rs3917615 |
hgdp | rs3917615 |
ensembl | rs3917615 |
geneview | rs3917615 |
scholar | rs3917615 |
rs3917615 | |
pharmgkb | rs3917615 |
gwascentral | rs3917615 |
openSNP | rs3917615 |
23andMe | rs3917615 |
SNPshot | rs3917615 |
SNPdbe | rs3917615 |
MSV3d | rs3917615 |
GWAS Ctlg | rs3917615 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25407675] Genetic variation in the tissue factor gene is associated with clinical outcome in severe sepsis patients