FAM186A c.6503+4907G>T

Variant ID: 12-50739205-C-A

NM_001145475.1(FAM186A):c.6503+4907G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Six novel susceptibility loci for coronary artery disease and cerebral infarction identified by longitudinal exome-wide association studies in a Japanese population.

Biomedical Reports
Yasukochi, Yoshiki Y; Sakuma, Jun J; Takeuchi, Ichiro I; Kato, Kimihiko K; Oguri, Mitsutoshi M; Fujimaki, Tetsuo T; Horibe, Hideki H; Yamada, Yoshiji Y
Publication Date: 2018-08

Variant appearance in text: rs4768872
PubMed Link: 29963304
Variant Present in the following documents:
  • Main text
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