TNC c.4033+1295A>G

Variant ID: 9-117823901-T-C

NM_002160.3(TNC):c.4033+1295A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.

Human Genetics
Minear, Mollie A MA; Crosslin, David R DR; Sutton, Beth S BS; Connelly, Jessica J JJ; Nelson, Sarah C SC; Gadson-Watson, Shera S; Wang, Tianyuan T; Seo, David D; Vance, Jeffrey M JM; Sketch, Michael H MH; Haynes, Carol C; Goldschmidt-Clermont, Pascal J PJ; Shah, Svati H SH; Kraus, William E WE; Hauser, Elizabeth R ER; Gregory, Simon G SG
Publication Date: 2011-06

Variant appearance in text: rs944225
PubMed Link: 21298289
Variant Present in the following documents:
  • Main text
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