NCAM1 c.52+37018T>C

Variant ID: 11-112869404-T-C

NM_181351.5(NCAM1):c.52+37018T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci.

Molecular Psychiatry
Deak, Joseph D JD; Zhou, Hang H; Galimberti, Marco M; Levey, Daniel F DF; Wendt, Frank R FR; Sanchez-Roige, Sandra S; Hatoum, Alexander S AS; Johnson, Emma C EC; Nunez, Yaira Z YZ; Demontis, Ditte D; Børglum, Anders D AD; Rajagopal, Veera M VM; Jennings, Mariela V MV; Kember, Rachel L RL; Justice, Amy C AC; Edenberg, Howard J HJ; Agrawal, Arpana A; Polimanti, Renato R; Kranzler, Henry R HR; Gelernter, Joel J
Publication Date: 2022-10

Variant appearance in text: rs1940701
PubMed Link: 35879402
Variant Present in the following documents:
  • Main text
  • 41380_2022_Article_1709.pdf
View BVdb publication page