rs62187992
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs62187992(A;A) |
Make rs62187992(A;G) |
Make rs62187992(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 212677971 |
is a | snp |
is | mentioned by |
dbSNP | rs62187992 |
dbSNP (classic) | rs62187992 |
ClinGen | rs62187992 |
ebi | rs62187992 |
HLI | rs62187992 |
Exac | rs62187992 |
Gnomad | rs62187992 |
Varsome | rs62187992 |
LitVar | rs62187992 |
Map | rs62187992 |
PheGenI | rs62187992 |
Biobank | rs62187992 |
1000 genomes | rs62187992 |
hgdp | rs62187992 |
ensembl | rs62187992 |
geneview | rs62187992 |
scholar | rs62187992 |
rs62187992 | |
pharmgkb | rs62187992 |
gwascentral | rs62187992 |
openSNP | rs62187992 |
23andMe | rs62187992 |
SNPshot | rs62187992 |
SNPdbe | rs62187992 |
MSV3d | rs62187992 |
GWAS Ctlg | rs62187992 |
Max Magnitude | 0 |
[PMID 27490645] Genetic variation 25.1 Mb upstream of tissue factor pathway inhibitor is associated with TFPI plasma levels and venous thromboembolism.