SEPT8 c.30+5749C>A

Variant ID: 5-132107051-G-T

NM_001098811.1(SEPT8):c.30+5749C>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus.

Plos Genetics
Weidinger, Stephan S; Gieger, Christian C; Rodriguez, Elke E; Baurecht, Hansjörg H; Mempel, Martin M; Klopp, Norman N; Gohlke, Henning H; Wagenpfeil, Stefan S; Ollert, Markus M; Ring, Johannes J; Behrendt, Heidrun H; Heinrich, Joachim J; Novak, Natalija N; Bieber, Thomas T; Krämer, Ursula U; Berdel, Dietrich D; von Berg, Andrea A; Bauer, Carl Peter CP; Herbarth, Olf O; Koletzko, Sibylle S; Prokisch, Holger H; Mehta, Divya D; Meitinger, Thomas T; Depner, Martin M; von Mutius, Erika E; Liang, Liming L; Moffatt, Miriam M; Cookson, William W; Kabesch, Michael M; Wichmann, H-Erich HE; Illig, Thomas T
Publication Date: 2008-08

Variant appearance in text: rs402959
PubMed Link: 18846228
Variant Present in the following documents:
View BVdb publication page



Genome-wide SNP typing reveals signatures of population history.

Genomics
Hughes, Austin L AL; Welch, Robert R; Puri, Vinita V; Matthews, Casey C; Haque, Kashif K; Chanock, Stephen J SJ; Yeager, Meredith M
Publication Date: 2008-07

Variant appearance in text: rs402959
PubMed Link: 18485661
Variant Present in the following documents:
  • Main text
View BVdb publication page