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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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
View BVdb publication page