SPI1 c.494-1299G>C

Variant ID: 11-47378396-C-G

NM_003120.2(SPI1):c.494-1299G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study.

Heart Rhythm
Lin, Honghuang H; Sinner, Moritz F MF; Brody, Jennifer A JA; Arking, Dan E DE; Lunetta, Kathryn L KL; Rienstra, Michiel M; Lubitz, Steven A SA; Magnani, Jared W JW; Sotoodehnia, Nona N; McKnight, Barbara B; McManus, David D DD; Boerwinkle, Eric E; Psaty, Bruce M BM; Rotter, Jerome I JI; Bis, Joshua C JC; Gibbs, Richard A RA; Muzny, Donna D; Kovar, Christie L CL; Morrison, Alanna C AC; Gupta, Mayetri M; Folsom, Aaron R AR; Kääb, Stefan S; Heckbert, Susan R SR; Alonso, Alvaro A; Ellinor, Patrick T PT; Benjamin, Emelia J EJ; ,
Publication Date: 2014-03

Variant appearance in text: rs10769256
PubMed Link: 24239840
Variant Present in the following documents:
  • Main text
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