MAGOH c.259-1425G>A

Variant ID: 1-53696051-C-T

NM_002370.3(MAGOH):c.259-1425G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.

American Journal Of Human Genetics
Shen, Gong-Qing GQ; Li, Lin L; Girelli, Domenico D; Seidelmann, Sara B SB; Rao, Shaoqi S; Fan, Chun C; Park, Jeong Euy JE; Xi, Quansheng Q; Li, Jing J; Hu, Ying Y; Olivieri, Oliviero O; Marchant, Kandice K; Barnard, John J; Corrocher, Roberto R; Elston, Robert R; Cassano, June J; Henderson, Susan S; Hazen, Stanley L SL; Plow, Edward F EF; Topol, Eric J EJ; Wang, Qing K QK
Publication Date: 2007-10

Variant appearance in text: rs10788949
PubMed Link: 17847002
Variant Present in the following documents:
  • Main text
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