rs2074597
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2074597(G;G) |
Make rs2074597(G;T) |
Make rs2074597(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 11637067 |
Gene | THSD7A |
is a | snp |
is | mentioned by |
dbSNP | rs2074597 |
dbSNP (classic) | rs2074597 |
ClinGen | rs2074597 |
ebi | rs2074597 |
HLI | rs2074597 |
Exac | rs2074597 |
Gnomad | rs2074597 |
Varsome | rs2074597 |
LitVar | rs2074597 |
Map | rs2074597 |
PheGenI | rs2074597 |
Biobank | rs2074597 |
1000 genomes | rs2074597 |
hgdp | rs2074597 |
ensembl | rs2074597 |
geneview | rs2074597 |
scholar | rs2074597 |
rs2074597 | |
pharmgkb | rs2074597 |
gwascentral | rs2074597 |
openSNP | rs2074597 |
23andMe | rs2074597 |
SNPshot | rs2074597 |
SNPdbe | rs2074597 |
MSV3d | rs2074597 |
GWAS Ctlg | rs2074597 |
GMAF | 0.3242 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 23742623] Genome-wide linkage scan in affected sibling pairs identifies novel susceptibility region for venous thromboembolism: Genetics In Familial Thrombosis (GIFT) study