SCN5A c.2437-293T>C

Variant ID: 3-38627825-A-G

NM_000335.4(SCN5A):c.2437-293T>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: SCN5A: 2437-293T>C; rs7645358
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs7645358
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



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: rs7645358
PubMed Link: 18676988
Variant Present in the following documents:
  • Main text
View BVdb publication page