rs516651
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs516651(C;C) |
Make rs516651(C;T) |
Make rs516651(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 231406910 |
Gene | EGLN1 |
is a | snp |
is | mentioned by |
dbSNP | rs516651 |
dbSNP (classic) | rs516651 |
ClinGen | rs516651 |
ebi | rs516651 |
HLI | rs516651 |
Exac | rs516651 |
Gnomad | rs516651 |
Varsome | rs516651 |
LitVar | rs516651 |
Map | rs516651 |
PheGenI | rs516651 |
Biobank | rs516651 |
1000 genomes | rs516651 |
hgdp | rs516651 |
ensembl | rs516651 |
geneview | rs516651 |
scholar | rs516651 |
rs516651 | |
pharmgkb | rs516651 |
gwascentral | rs516651 |
openSNP | rs516651 |
23andMe | rs516651 |
SNPshot | rs516651 |
SNPdbe | rs516651 |
MSV3d | rs516651 |
GWAS Ctlg | rs516651 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 27515179] Hypoxia inducible factor-1 alpha and prolinhydroxlase 2 polymorphisms in patients with severe sepsis: a prospective observational trial.
[PMID 28613249] Hypoxia Inducible Factor-2 Alpha and Prolinhydroxylase 2 Polymorphisms in Patients with Acute Respiratory Distress Syndrome (ARDS).