CSMD1 c.1010-34658T>C

Variant ID: 8-3508977-A-G

NM_033225.5(CSMD1):c.1010-34658T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A genome-wide investigation of SNPs and CNVs in schizophrenia.

Plos Genetics
Need, Anna C AC; Ge, Dongliang D; Weale, Michael E ME; Maia, Jessica J; Feng, Sheng S; Heinzen, Erin L EL; Shianna, Kevin V KV; Yoon, Woohyun W; Kasperaviciūte, Dalia D; Gennarelli, Massimo M; Strittmatter, Warren J WJ; Bonvicini, Cristian C; Rossi, Giuseppe G; Jayathilake, Karu K; Cola, Philip A PA; McEvoy, Joseph P JP; Keefe, Richard S E RS; Fisher, Elizabeth M C EM; St Jean, Pamela L PL; Giegling, Ina I; Hartmann, Annette M AM; Möller, Hans-Jürgen HJ; Ruppert, Andreas A; Fraser, Gillian G; Crombie, Caroline C; Middleton, Lefkos T LT; St Clair, David D; Roses, Allen D AD; Muglia, Pierandrea P; Francks, Clyde C; Rujescu, Dan D; Meltzer, Herbert Y HY; Goldstein, David B DB
Publication Date: 2009-02

Variant appearance in text: rs1586030
PubMed Link: 19197363
Variant Present in the following documents:
  • Main text
  • pgen.1000373.pdf
View BVdb publication page