ELAVL2 c.230-5277T>C

Variant ID: 9-23736400-A-G

NM_004432.3(ELAVL2):c.230-5277T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools.

Brain : A Journal Of Neurology
Bahrami, Shahram S; Hindley, Guy G; Winsvold, Bendik Slagsvold BS; O'Connell, Kevin S KS; Frei, Oleksandr O; Shadrin, Alexey A; Cheng, Weiqiu W; Bettella, Francesco F; Rødevand, Linn L; Odegaard, Ketil J KJ; Fan, Chun C CC; Pirinen, Matti J MJ; Hautakangas, Heidi M HM; , ; Dale, Anders M AM; Djurovic, Srdjan S; Smeland, Olav B OB; Andreassen, Ole A OA
Publication Date: 2022-03-29

Variant appearance in text: rs10119773
PubMed Link: 34273149
Variant Present in the following documents:
  • Main text
  • awab267.pdf
View BVdb publication page



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: rs10119773
PubMed Link: 29500382
Variant Present in the following documents:
  • 41467_2018_3242_MOESM2_ESM.pdf
View BVdb publication page