TNR c.2053+382G>C

Variant ID: 1-175335962-C-G

NM_003285.2(TNR):c.2053+382G>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Combinations of Genetic Data Present in Bipolar Patients, but Absent in Control Persons.

Plos One
Mellerup, Erling E; Andreassen, Ole A OA; Bennike, Bente B; Dam, Henrik H; Djurovic, Srdjan S; Hansen, Thomas T; Jorgensen, Martin Balslev MB; Kessing, Lars Vedel LV; Koefoed, Pernille P; Melle, Ingrid I; Mors, Ole O; Werge, Thomas T; Moeller, Gert Lykke GL
Publication Date: 2015

Variant appearance in text: rs2239821
PubMed Link: 26587987
Variant Present in the following documents:
  • pone.0143432.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: rs2239821
PubMed Link: 23028568
Variant Present in the following documents:
  • Main text
  • pone.0044623.pdf
View BVdb publication page