TTN c.2077-382A>G

Variant ID: 2-179651250-T-C

NM_001267550.1(TTN):c.2077-382A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.

Bmc Medical Genetics
Larson, Martin G MG; Atwood, Larry D LD; Benjamin, Emelia J EJ; Cupples, L Adrienne LA; D'Agostino, Ralph B RB; Fox, Caroline S CS; Govindaraju, Diddahally R DR; Guo, Chao-Yu CY; Heard-Costa, Nancy L NL; Hwang, Shih-Jen SJ; Murabito, Joanne M JM; Newton-Cheh, Christopher C; O'Donnell, Christopher J CJ; Seshadri, Sudha S; Vasan, Ramachandran S RS; Wang, Thomas J TJ; Wolf, Philip A PA; Levy, Daniel D
Publication Date: 2007-09-19

Variant appearance in text: rs10497521
PubMed Link: 17903304
Variant Present in the following documents:
  • Main text
  • 1471-2350-8-S1-S5.pdf
View BVdb publication page