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rs516651

From SNPedia

Orientationplus
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
ebirs516651
HLIrs516651
Exacrs516651
Varsomers516651
Maprs516651
PheGenIrs516651
hapmaprs516651
1000 genomesrs516651
hgdprs516651
ensemblrs516651
gopubmedrs516651
geneviewrs516651
scholarrs516651
googlers516651
pharmgkbrs516651
gwascentralrs516651
openSNPrs516651
23andMers516651
23andMe allrs516651
SNP Nexus

SNPshotrs516651
SNPdbers516651
MSV3drs516651
GWAS Ctlgrs516651
Max Magnitude
? (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.