CD36 c.158_159insG ;(p.N53Kfs*4)

Variant ID: 7-80285893-A-AG

NM_001001548.2(CD36):c.158_159insG;(p.N53Kfs*4)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.

American Journal Of Human Genetics
Auer, Paul L PL; Johnsen, Jill M JM; Johnson, Andrew D AD; Logsdon, Benjamin A BA; Lange, Leslie A LA; Nalls, Michael A MA; Zhang, Guosheng G; Franceschini, Nora N; Fox, Keolu K; Lange, Ethan M EM; Rich, Stephen S SS; O'Donnell, Christopher J CJ; Jackson, Rebecca D RD; Wallace, Robert B RB; Chen, Zhao Z; Graubert, Timothy A TA; Wilson, James G JG; Tang, Hua H; Lettre, Guillaume G; Reiner, Alex P AP; Ganesh, Santhi K SK; Li, Yun Y
Publication Date: 2012-11-02

Variant appearance in text: CD36: 158_159insG; Asn53Lysfs; rs3211862
PubMed Link: 23103231
Variant Present in the following documents:
  • Main text
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