rs1799808
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1799808(C;C) |
Make rs1799808(C;T) |
Make rs1799808(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 127418286 |
Gene | PROC |
is a | snp |
is | mentioned by |
dbSNP | rs1799808 |
dbSNP (classic) | rs1799808 |
ClinGen | rs1799808 |
ebi | rs1799808 |
HLI | rs1799808 |
Exac | rs1799808 |
Gnomad | rs1799808 |
Varsome | rs1799808 |
LitVar | rs1799808 |
Map | rs1799808 |
PheGenI | rs1799808 |
Biobank | rs1799808 |
1000 genomes | rs1799808 |
hgdp | rs1799808 |
ensembl | rs1799808 |
geneview | rs1799808 |
scholar | rs1799808 |
rs1799808 | |
pharmgkb | rs1799808 |
gwascentral | rs1799808 |
openSNP | rs1799808 |
23andMe | rs1799808 |
SNPshot | rs1799808 |
SNPdbe | rs1799808 |
MSV3d | rs1799808 |
GWAS Ctlg | rs1799808 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25376901] Genetic Markers Associated With Plasma Protein C Level in African Americans: The Atherosclerosis Risk in Communities (ARIC) Study
[PMID 24816905] Single nucleotide variants in the protein C pathway and mortality in dialysis patients