CNTNAP2 c.3010+852C>T

Variant ID: 7-147870422-C-T

NM_014141.5(CNTNAP2):c.3010+852C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Combinations of Genetic Variants Occurring Exclusively in Patients.

Computational And Structural Biotechnology Journal
Mellerup, Erling E; Møller, Gert Lykke GL
Publication Date: 2017

Variant appearance in text: rs2972112
PubMed Link: 28377798
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



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: rs2972112
PubMed Link: 26587987
Variant Present in the following documents:
  • Main text
  • 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: rs2972112
PubMed Link: 23028568
Variant Present in the following documents:
  • Main text
  • pone.0044623.pdf
View BVdb publication page