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SCN1A c.265-7015A>G
Variant ID: 2-166922213-T-C
NM_001165963.1(
SCN1A
):c.265-7015A>G
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:
Meta-analysis of genome-wide association for migraine in six population-based European cohorts.
European Journal Of Human Genetics : Ejhg
Ligthart, Lannie L; de Vries, Boukje B; Smith, Albert V AV; Ikram, M Arfan MA; Amin, Najaf N; Hottenga, Jouke-Jan JJ; Koelewijn, Stephany C SC; Kattenberg, V Mathijs VM; de Moor, Marleen H M MH; Janssens, A Cecile J W AC; Aulchenko, Yurii S YS; Oostra, Ben A BA; de Geus, Eco J C EJ; Smit, Johannes H JH; Zitman, Frans G FG; Uitterlinden, André G AG; Hofman, Albert A; Willemsen, Gonneke G; Nyholt, Dale R DR; Montgomery, Grant W GW; Terwindt, Gisela M GM; Gudnason, Vilmundur V; Penninx, Brenda W J H BW; Breteler, Monique M; Ferrari, Michel D MD; Launer, Lenore J LJ; van Duijn, Cornelia M CM; van den Maagdenberg, Arn M J M AM; Boomsma, Dorret I DI
Publication Date: 2011-08
Variant appearance in text: rs12151636
PubMed Link:
21448238
Variant Present in the following documents:
Main text
ejhg201148a.pdf
View BVdb publication page