rs2069912
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | sepsis risk in East Asians | |
(C;T) | sepsis risk in East Asians | |
(T;T) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 127420615 |
Gene | PROC |
is a | snp |
is | mentioned by |
dbSNP | rs2069912 |
dbSNP (classic) | rs2069912 |
ClinGen | rs2069912 |
ebi | rs2069912 |
HLI | rs2069912 |
Exac | rs2069912 |
Gnomad | rs2069912 |
Varsome | rs2069912 |
LitVar | rs2069912 |
Map | rs2069912 |
PheGenI | rs2069912 |
Biobank | rs2069912 |
1000 genomes | rs2069912 |
hgdp | rs2069912 |
ensembl | rs2069912 |
geneview | rs2069912 |
scholar | rs2069912 |
rs2069912 | |
pharmgkb | rs2069912 |
gwascentral | rs2069912 |
openSNP | rs2069912 |
23andMe | rs2069912 |
SNPshot | rs2069912 |
SNPdbe | rs2069912 |
MSV3d | rs2069912 |
GWAS Ctlg | rs2069912 |
GMAF | 0.3159 |
Max Magnitude | 0 |
The rs2069912(C) allele is associated with severe sepsis and thus increased risk of death and organ dysfunction based on a study of 100 North American East Asians. The original report of this association was (also) in Chinese patients.[PMID 18496716]
[PMID 19941661] A MIF haplotype is associated with the outcome of patients with severe sepsis: a case control study.