CNTNAP2 c.1670+45005G>A

Variant ID: 7-147137877-G-A

NM_014141.5(CNTNAP2):c.1670+45005G>A

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

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: rs7803315
PubMed Link: 23028568
Variant Present in the following documents:
  • Main text
  • pone.0044623.pdf
View BVdb publication page