CACNG2 c.211+6780A>T

Variant ID: 22-37091631-T-A

NM_006078.3(CACNG2):c.211+6780A>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Response to Belgard et al.

Molecular Psychiatry
Skafidas, E E; Testa, R R; Zantomio, D D; Chana, G G; Everall, I P IP; Pantelis, C C
Publication Date: 2014-04

Variant appearance in text: rs2179871
PubMed Link: 24419040
Variant Present in the following documents:
  • Main text
  • mp2013186a.pdf
View BVdb publication page



Connection between genetic and clinical data in bipolar disorder.

Plos One
Mellerup, Erling E; Andreassen, Ole O; Bennike, Bente B; Dam, Henrik H; Djurovic, Srdjan S; Durovic, Srdjan S; Hansen, Thomas T; Melle, Ingrid I; Møller, Gert Lykke GL; Mors, Ole O; Koefoed, Pernille P
Publication Date: 2012

Variant appearance in text: rs2179871
PubMed Link: 23028568
Variant Present in the following documents:
  • Main text
  • pone.0044623.pdf
View BVdb publication page



Combinations of SNPs related to signal transduction in bipolar disorder.

Plos One
Koefoed, Pernille P; Andreassen, Ole A OA; Bennike, Bente B; Dam, Henrik H; Djurovic, Srdjan S; Hansen, Thomas T; Jorgensen, Martin Balslev MB; Kessing, Lars Vedel LV; Melle, Ingrid I; Møller, Gert Lykke GL; Mors, Ole O; Werge, Thomas T; Mellerup, Erling E
Publication Date: 2011

Variant appearance in text: rs2179871
PubMed Link: 21897858
Variant Present in the following documents:
  • Main text
  • pone.0023812.pdf
View BVdb publication page