F2 c.79+7G>A

Variant ID: 11-46740871-G-A

NM_000506.3(F2):c.79+7G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.

Human Molecular Genetics
Drenos, Fotios F; Talmud, Philippa J PJ; Casas, Juan P JP; Smeeth, Liam L; Palmen, Jutta J; Humphries, Steve E SE; Hingorani, Aroon D AD
Publication Date: 2009-06-15

Variant appearance in text: rs3136431
PubMed Link: 19336475
Variant Present in the following documents:
  • ddp159_1.pdf
View BVdb publication page



Genetic associations with thalidomide mediated venous thrombotic events in myeloma identified using targeted genotyping.

Blood
Johnson, David C DC; Corthals, Sophie S; Ramos, Christine C; Hoering, Antje A; Cocks, Kim K; Dickens, Nicholas J NJ; Haessler, Jeff J; Goldschmidt, Harmut H; Child, J Anthony JA; Bell, Sue E SE; Jackson, Graham G; Baris, Dalsu D; Rajkumar, S Vincent SV; Davies, Faith E FE; Durie, Brian G M BG; Crowley, John J; Sonneveld, Pieter P; Van Ness, Brian B; Morgan, Gareth J GJ
Publication Date: 2008-12-15

Variant appearance in text: rs3136431
PubMed Link: 18805967
Variant Present in the following documents:
  • Main text
View BVdb publication page