CNTN5 c.56-118969T>C

Variant ID: 11-99571306-T-C

NM_014361.3(CNTN5):c.56-118969T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Item-level analyses reveal genetic heterogeneity in neuroticism.

Nature Communications
Nagel, Mats M; Watanabe, Kyoko K; Stringer, Sven S; Posthuma, Danielle D; van der Sluis, Sophie S
Publication Date: 2018-03-02

Variant appearance in text: rs628246
PubMed Link: 29500382
Variant Present in the following documents:
  • 41467_2018_3242_MOESM2_ESM.pdf
View BVdb publication page