HMOX1 c.636+448G>A

Variant ID: 22-35783617-G-A

NM_002133.2(HMOX1):c.636+448G>A

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Interaction between arsenic exposure from drinking water and genetic polymorphisms on cardiovascular disease in Bangladesh: a prospective case-cohort study.

Environmental Health Perspectives
Wu, Fen F; Jasmine, Farzana F; Kibriya, Muhammad G MG; Liu, Mengling M; Cheng, Xin X; Parvez, Faruque F; Islam, Tariqul T; Ahmed, Alauddin A; Rakibuz-Zaman, Muhammad M; Jiang, Jieying J; Roy, Shantanu S; Paul-Brutus, Rachelle R; Slavkovich, Vesna V; Islam, Tariqul T; Levy, Diane D; VanderWeele, Tyler J TJ; Pierce, Brandon L BL; Graziano, Joseph H JH; Ahsan, Habibul H; Chen, Yu Y
Publication Date: 2015-05

Variant appearance in text: rs11912889
PubMed Link: 25575156
Variant Present in the following documents:
  • ehp.1307883.s001.508.pdf
View BVdb publication page



HMOX1 gene promoter alleles and high HO-1 levels are associated with severe malaria in Gambian children.

Plos Pathogens
Walther, Michael M; De Caul, Adam A; Aka, Peter P; Njie, Madi M; Amambua-Ngwa, Alfred A; Walther, Brigitte B; Predazzi, Irene M IM; Cunnington, Aubrey A; Deininger, Susanne S; Takem, Ebako N EN; Ebonyi, Augustine A; Weis, Sebastian S; Walton, Robert R; Rowland-Jones, Sarah S; Sirugo, Giorgio G; Williams, Scott M SM; Conway, David J DJ
Publication Date: 2012

Variant appearance in text: rs11912889
PubMed Link: 22438807
Variant Present in the following documents:
  • Main text
  • ppat.1002579.pdf
View BVdb publication page



Transforming growth factor beta 2 and heme oxygenase 1 genes are risk factors for the cerebral malaria syndrome in Angolan children.

Plos One
Sambo, Maria Rosário MR; Trovoada, Maria Jesus MJ; Benchimol, Carla C; Quinhentos, Vatúsia V; Gonçalves, Lígia L; Velosa, Rute R; Marques, Maria Isabel MI; Sepúlveda, Nuno N; Clark, Taane G TG; Mustafa, Stefan S; Wagner, Oswald O; Coutinho, António A; Penha-Gonçalves, Carlos C
Publication Date: 2010-06-16

Variant appearance in text: rs11912889
PubMed Link: 20585394
Variant Present in the following documents:
  • Main text
  • pone.0011141.pdf
View BVdb publication page



A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.

British Journal Of Haematology
Constantine, Clare C CC; Anderson, Greg J GJ; Vulpe, Chris D CD; McLaren, Christine E CE; Bahlo, Melanie M; Yeap, Heng Lin HL; Gertig, Dorota M DM; Osborne, Nicholas J NJ; Bertalli, Nadine A NA; Beckman, Kenneth B KB; Chen, Victoria V; Matak, Pavel P; McKie, Andrew T AT; Delatycki, Martin B MB; Olynyk, John K JK; English, Dallas R DR; Southey, Melissa C MC; Giles, Graham G GG; Hopper, John L JL; Allen, Katrina J KJ; Gurrin, Lyle C LC
Publication Date: 2009-10

Variant appearance in text: rs11912889
PubMed Link: 19673882
Variant Present in the following documents:
  • Main text
View BVdb publication page



Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.

Human Molecular Genetics
Drenos, Fotios F; Talmud, Philippa J PJ; Casas, Juan P JP; Smeeth, Liam L; Palmen, Jutta J; Humphries, Steve E SE; Hingorani, Aroon D AD
Publication Date: 2009-06-15

Variant appearance in text: rs11912889
PubMed Link: 19336475
Variant Present in the following documents:
  • ddp159_1.pdf
View BVdb publication page