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rs2071747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2071747(C;C)
Make rs2071747(C;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position35381192
GeneHMOX1
is asnp
is mentioned by
dbSNPrs2071747
ebirs2071747
HLIrs2071747
Exacrs2071747
Varsomers2071747
Maprs2071747
PheGenIrs2071747
hapmaprs2071747
1000 genomesrs2071747
hgdprs2071747
ensemblrs2071747
gopubmedrs2071747
geneviewrs2071747
scholarrs2071747
googlers2071747
pharmgkbrs2071747
gwascentralrs2071747
openSNPrs2071747
23andMers2071747
23andMe allrs2071747
SNP Nexus

SNPshotrs2071747
SNPdbers2071747
MSV3drs2071747
GWAS Ctlgrs2071747
GMAF0.05005
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 21647550OA-icon.png] An association between polymorphism of the heme oxygenase-1 and -2 genes and age-related macular degeneration


[PMID 18640487OA-icon.png] Association of donor inflammation- and apoptosis-related genotypes and delayed allograft function after kidney transplantation.


[PMID 19406964OA-icon.png] Association of genetic variants with chronic kidney disease in Japanese individuals.


GET Evidence
HMOX1-D7H
aa_change Asp7His
aa_change_short D7H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0291746
summary



[PMID 26313808OA-icon.png] Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome


[PMID 26868429] Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis.