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rs5995098

From SNPedia

Orientationplus
Stabilizedplus
Make rs5995098(C;C)
Make rs5995098(C;G)
Make rs5995098(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position35391174
GeneHMOX1
is asnp
is mentioned by
dbSNPrs5995098
dbSNP (classic)rs5995098
ClinGenrs5995098
ebirs5995098
HLIrs5995098
Exacrs5995098
Gnomadrs5995098
Varsomers5995098
LitVarrs5995098
Maprs5995098
PheGenIrs5995098
Biobankrs5995098
1000 genomesrs5995098
hgdprs5995098
ensemblrs5995098
geneviewrs5995098
scholarrs5995098
googlers5995098
pharmgkbrs5995098
gwascentralrs5995098
openSNPrs5995098
23andMers5995098
SNPshotrs5995098
SNPdbers5995098
MSV3drs5995098
GWAS Ctlgrs5995098
GMAF0.2994
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 20190330] HMOX1 and GST variants modify attenuation of FEF25-75% decline due to PM10 reduction


[PMID 32141648OA-icon.png] Association of heme oxygenase-1 single nucleotide polymorphisms with susceptibility to tuberculosis in Chinese Han population.