MTHFD1L c.2125+6838C>A

Variant ID: 6-151300032-C-A

NM_015440.4(MTHFD1L):c.2125+6838C>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts.

Genetic Epidemiology
Karvanen, Juha J; Silander, Kaisa K; Kee, Frank F; Tiret, Laurence L; Salomaa, Veikko V; Kuulasmaa, Kari K; Wiklund, Per-Gunnar PG; Virtamo, Jarmo J; Saarela, Olli O; Perret, Claire C; Perola, Markus M; Peltonen, Leena L; Cambien, Francois F; Erdmann, Jeanette J; Samani, Nilesh J NJ; Schunkert, Heribert H; Evans, Alun A; ,
Publication Date: 2009-04

Variant appearance in text: rs12525353
PubMed Link: 18979498
Variant Present in the following documents:
  • Main text
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