ECE1 c.762+172G>A

Variant ID: 1-21585014-C-T

NM_001397.2(ECE1):c.762+172G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: rs212527
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
View BVdb publication page



Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.

Blood
Baldwin, Clinton C; Nolan, Vikki G VG; Wyszynski, Diego F DF; Ma, Qian-Li QL; Sebastiani, Paola P; Embury, Stephen H SH; Bisbee, Alice A; Farrell, John J; Farrer, Lindsay L; Steinberg, Martin H MH
Publication Date: 2005-07-01

Variant appearance in text: rs212527
PubMed Link: 15784727
Variant Present in the following documents:
  • Main text
View BVdb publication page