rs5853517
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs5853517(-;-) |
Make rs5853517(-;T) |
Make rs5853517(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 151339797 |
Gene | MED12L, P2RY12 |
is a | snp |
is | mentioned by |
dbSNP | rs5853517 |
dbSNP (classic) | rs5853517 |
ClinGen | rs5853517 |
ebi | rs5853517 |
HLI | rs5853517 |
Exac | rs5853517 |
Gnomad | rs5853517 |
Varsome | rs5853517 |
LitVar | rs5853517 |
Map | rs5853517 |
PheGenI | rs5853517 |
Biobank | rs5853517 |
1000 genomes | rs5853517 |
hgdp | rs5853517 |
ensembl | rs5853517 |
geneview | rs5853517 |
scholar | rs5853517 |
rs5853517 | |
pharmgkb | rs5853517 |
gwascentral | rs5853517 |
openSNP | rs5853517 |
23andMe | rs5853517 |
SNPshot | rs5853517 |
SNPdbe | rs5853517 |
MSV3d | rs5853517 |
GWAS Ctlg | rs5853517 |
GMAF | 0.1515 |
Max Magnitude | 0 |
[PMID 17707382] rs10935838, rs2046934, rs5853517, and rs6809699 venous thromboembolism lower risk of incident DVT/PE as compared to the reference haplotype H1 (odds ratio=0.50, 95% CI=0.27-0.93, p=0.028)