Have questions? Visit https://www.reddit.com/r/SNPedia

rs2270363

From SNPedia

Orientationplus
Stabilizedplus
Make rs2270363(A;A)
Make rs2270363(A;G)
Make rs2270363(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position4476291
GeneHMOX2, NMRAL1
is asnp
is mentioned by
dbSNPrs2270363
ebirs2270363
HLIrs2270363
Exacrs2270363
Varsomers2270363
Maprs2270363
PheGenIrs2270363
hapmaprs2270363
1000 genomesrs2270363
hgdprs2270363
ensemblrs2270363
gopubmedrs2270363
geneviewrs2270363
scholarrs2270363
googlers2270363
pharmgkbrs2270363
gwascentralrs2270363
openSNPrs2270363
23andMers2270363
23andMe allrs2270363
SNP Nexus

SNPshotrs2270363
SNPdbers2270363
MSV3drs2270363
GWAS Ctlgrs2270363
GMAF0.2663
Max Magnitude
? (A;A) (A;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 21709601] A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease

[PMID 26313808] 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.