TOX c.693+2349A>G

Variant ID: 8-59761734-T-C

NM_014729.2(TOX):c.693+2349A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

Genomics Insights
Driss, A A; Asare, K O KO; Hibbert, J M JM; Gee, B E BE; Adamkiewicz, T V TV; Stiles, J K JK
Publication Date: 2009-07-30

Variant appearance in text: rs1349115
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
View BVdb publication page



A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples.

Bmc Genetics
Sebastiani, Paola P; Zhao, Zhenming Z; Abad-Grau, Maria M MM; Riva, Alberto A; Hartley, Stephen W SW; Sedgewick, Amanda E AE; Doria, Alessandro A; Montano, Monty M; Melista, Efthymia E; Terry, Dellara D; Perls, Thomas T TT; Steinberg, Martin H MH; Baldwin, Clinton T CT
Publication Date: 2008-01-14

Variant appearance in text: rs1349115
PubMed Link: 18194558
Variant Present in the following documents:
  • Main text
  • 1471-2156-9-6.pdf
View BVdb publication page