SCN2A c.387-1653G>A

Variant ID: 2-166162705-G-A

NM_001040142.1(SCN2A):c.387-1653G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: rs12469667
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: rs12469667
PubMed Link: 21897858
Variant Present in the following documents:
  • Main text
  • pone.0023812.pdf
View BVdb publication page