rs2071747

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs2071747(C;C)

Make rs2071747(C;G)

Reference

GRCh38 38.1/141

Chromosome

22

Position

35381192

Gene

HMOX1

is a	snp
is	mentioned by
dbSNP	rs2071747
dbSNP (classic)	rs2071747
ClinGen	rs2071747
ebi	rs2071747
HLI	rs2071747
Exac	rs2071747
Gnomad	rs2071747
Varsome	rs2071747
LitVar	rs2071747
Map	rs2071747
PheGenI	rs2071747
Biobank	rs2071747
1000 genomes	rs2071747
hgdp	rs2071747
ensembl	rs2071747
geneview	rs2071747
scholar	rs2071747
google	rs2071747
pharmgkb	rs2071747
gwascentral	rs2071747
openSNP	rs2071747
23andMe	rs2071747
SNPshot	rs2071747
SNPdbe	rs2071747
MSV3d	rs2071747
GWAS Ctlg	rs2071747

GMAF

0.05005

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 21647550] An association between polymorphism of the heme oxygenase-1 and -2 genes and age-related macular degeneration

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

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

[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.

[PMID 28179208] Association between a heme oxygenase-2 genetic variant and risk of Parkinson's disease in Han Chinese.

[PMID 28276576] Delta-amino-levulinic acid dehydratase gene and essential tremor.