rs2069951
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2069951(A;A) |
Make rs2069951(A;G) |
Make rs2069951(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 20 |
Position | 35175961 |
Gene | PROCR |
is a | snp |
is | mentioned by |
dbSNP | rs2069951 |
dbSNP (classic) | rs2069951 |
ClinGen | rs2069951 |
ebi | rs2069951 |
HLI | rs2069951 |
Exac | rs2069951 |
Gnomad | rs2069951 |
Varsome | rs2069951 |
LitVar | rs2069951 |
Map | rs2069951 |
PheGenI | rs2069951 |
Biobank | rs2069951 |
1000 genomes | rs2069951 |
hgdp | rs2069951 |
ensembl | rs2069951 |
geneview | rs2069951 |
scholar | rs2069951 |
rs2069951 | |
pharmgkb | rs2069951 |
gwascentral | rs2069951 |
openSNP | rs2069951 |
23andMe | rs2069951 |
SNPshot | rs2069951 |
SNPdbe | rs2069951 |
MSV3d | rs2069951 |
GWAS Ctlg | rs2069951 |
Max Magnitude | 0 |
[PMID 24816905] Single nucleotide variants in the protein C pathway and mortality in dialysis patients
[PMID 30383853] Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke.