SCN5A c.-52-6368G>C

Variant ID: 3-38681218-C-G

NM_000335.4(SCN5A):c.-52-6368G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A high-density association screen of 155 ion transport genes for involvement with common migraine.

Human Molecular Genetics
Nyholt, Dale R DR; LaForge, K Steven KS; Kallela, Mikko M; Alakurtti, Kirsi K; Anttila, Verneri V; Färkkilä, Markus M; Hämaläinen, Eija E; Kaprio, Jaakko J; Kaunisto, Mari A MA; Heath, Andrew C AC; Montgomery, Grant W GW; Göbel, Hartmut H; Todt, Unda U; Ferrari, Michel D MD; Launer, Lenore J LJ; Frants, Rune R RR; Terwindt, Gisela M GM; de Vries, Boukje B; Verschuren, W M Monique WM; Brand, Jan J; Freilinger, Tobias T; Pfaffenrath, Volker V; Straube, Andreas A; Ballinger, Dennis G DG; Zhan, Yiping Y; Daly, Mark J MJ; Cox, David R DR; Dichgans, Martin M; van den Maagdenberg, Arn M J M AM; Kubisch, Christian C; Martin, Nicholas G NG; Wessman, Maija M; Peltonen, Leena L; Palotie, Aarno A
Publication Date: 2008-11-01

Variant appearance in text: rs9311195
PubMed Link: 18676988
Variant Present in the following documents:
  • Main text
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