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rs516651

From SNPedia

Orientationplus
Stabilizedplus
Make rs516651(C;C)
Make rs516651(C;T)
Make rs516651(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position231406910
GeneEGLN1
is asnp
is mentioned by
dbSNPrs516651
dbSNP (classic)rs516651
ClinGenrs516651
ebirs516651
HLIrs516651
Exacrs516651
Gnomadrs516651
Varsomers516651
LitVarrs516651
Maprs516651
PheGenIrs516651
Biobankrs516651
1000 genomesrs516651
hgdprs516651
ensemblrs516651
geneviewrs516651
scholarrs516651
googlers516651
pharmgkbrs516651
gwascentralrs516651
openSNPrs516651
23andMers516651
SNPshotrs516651
SNPdbers516651
MSV3drs516651
GWAS Ctlgrs516651
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 27515179OA-icon.png] Hypoxia inducible factor-1 alpha and prolinhydroxlase 2 polymorphisms in patients with severe sepsis: a prospective observational trial.

[PMID 28613249OA-icon.png] Hypoxia Inducible Factor-2 Alpha and Prolinhydroxylase 2 Polymorphisms in Patients with Acute Respiratory Distress Syndrome (ARDS).