CSMD1 c.302+27530C>T

Variant ID: 8-4467334-G-A

NM_033225.5(CSMD1):c.302+27530C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic regulation of Nrxn1 [corrected] expression: an integrative cross-species analysis of schizophrenia candidate genes.

Translational Psychiatry
Mozhui, K K; Wang, X X; Chen, J J; Mulligan, M K MK; Li, Z Z; Ingles, J J; Chen, X X; Lu, L L; Williams, R W RW
Publication Date: 2011-07-26

Variant appearance in text: rs2725045
PubMed Link: 22832527
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants on chromosome 6p22.1 are associated with schizophrenia.

Nature
Shi, Jianxin J; Levinson, Douglas F DF; Duan, Jubao J; Sanders, Alan R AR; Zheng, Yonglan Y; Pe'er, Itsik I; Dudbridge, Frank F; Holmans, Peter A PA; Whittemore, Alice S AS; Mowry, Bryan J BJ; Olincy, Ann A; Amin, Farooq F; Cloninger, C Robert CR; Silverman, Jeremy M JM; Buccola, Nancy G NG; Byerley, William F WF; Black, Donald W DW; Crowe, Raymond R RR; Oksenberg, Jorge R JR; Mirel, Daniel B DB; Kendler, Kenneth S KS; Freedman, Robert R; Gejman, Pablo V PV
Publication Date: 2009-08-06

Variant appearance in text: rs2725045
PubMed Link: 19571809
Variant Present in the following documents:
View BVdb publication page