ECE1 c.616-329A>G

Variant ID: 1-21585661-T-C

NM_001397.2(ECE1):c.616-329A>G

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Association of Endothelin-Converting Enzyme and Endothelin-1 Gene Polymorphisms with Essential Hypertension in Malay Ethnics.

Genetics Research
Salim, Elnaz E; Ramachandran, Vasudevan V; Ansari, Neda N; Ismail, Patimah P; Mohamed, Mohd Hazmi MH; Mohamad, Nur Afiqah NA; Inche Mat, Liyana Najwa LN
Publication Date: 2022

Variant appearance in text: rs212528
PubMed Link: 35645613
Variant Present in the following documents:
  • GR2022-9129960.pdf
View BVdb publication page



Association of ECE1 gene polymorphisms and essential hypertension risk in the Northern Han Chinese: A case-control study.

Molecular Genetics & Genomic Medicine
Wang, Hao H; Liu, Jielin J; Liu, Kuo K; Liu, Ya Y; Wen, Jie J; Wang, Zuoguang Z; Wen, Shaojun S
Publication Date: 2020-04

Variant appearance in text: ECE1: 616-329A>G; rs212528
PubMed Link: 32107880
Variant Present in the following documents:
  • Main text
  • MGG3-8-e1188.pdf
View BVdb publication page



Association between ECE1 gene polymorphisms and risk of intracerebral haemorrhage.

The Journal Of International Medical Research
Zeng, Yi Y; Ma, Mingming M; Liu, Baoqiong B; Xia, Jian J; Xu, Hongwei H; Liu, Yunhai Y; Du, Xiaoping X; Hu, Zhiping Z; Yang, Qidong Q; Zhang, Le L
Publication Date: 2016-06

Variant appearance in text: rs212528
PubMed Link: 27036146
Variant Present in the following documents:
  • Main text
  • 10.1177_0300060516635385.pdf
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The role of the kallikrein-kinin system genes in the salt sensitivity of blood pressure: the GenSalt Study.

American Journal Of Epidemiology
Gu, Dongfeng D; Zhao, Qi Q; Kelly, Tanika N TN; Hixson, James E JE; Rao, Dabeeru C DC; Cao, Jie J; Chen, Jing J; Li, Jianxin J; Chen, Jichun J; Ji, Xu X; Hu, Dongsheng D; Wang, Xushan X; Liu, De-Pei DP; He, Jiang J
Publication Date: 2012-10-01

Variant appearance in text: rs212528
PubMed Link: 23035147
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic predictors for stroke in children with sickle cell anemia.

Blood
Flanagan, Jonathan M JM; Frohlich, Denise M DM; Howard, Thad A TA; Schultz, William H WH; Driscoll, Catherine C; Nagasubramanian, Ramamoorthy R; Mortier, Nicole A NA; Kimble, Amy C AC; Aygun, Banu B; Adams, Robert J RJ; Helms, Ronald W RW; Ware, Russell E RE
Publication Date: 2011-06-16

Variant appearance in text: rs212528
PubMed Link: 21515823
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

Genomics Insights
Driss, A A; Asare, K O KO; Hibbert, J M JM; Gee, B E BE; Adamkiewicz, T V TV; Stiles, J K JK
Publication Date: 2009-07-30

Variant appearance in text: rs212528
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
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Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia.

Nature Genetics
Sebastiani, Paola P; Ramoni, Marco F MF; Nolan, Vikki V; Baldwin, Clinton T CT; Steinberg, Martin H MH
Publication Date: 2005-04

Variant appearance in text: rs212528
PubMed Link: 15778708
Variant Present in the following documents:
  • Main text
View BVdb publication page