THSD7A c.1822+21466A>G

Variant ID: 7-11559580-T-C

NM_015204.2(THSD7A):c.1822+21466A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate.

Plos Genetics
Andreassen, Ole A OA; Thompson, Wesley K WK; Schork, Andrew J AJ; Ripke, Stephan S; Mattingsdal, Morten M; Kelsoe, John R JR; Kendler, Kenneth S KS; O'Donovan, Michael C MC; Rujescu, Dan D; Werge, Thomas T; Sklar, Pamela P; , ; , ; Roddey, J Cooper JC; Chen, Chi-Hua CH; McEvoy, Linda L; Desikan, Rahul S RS; Djurovic, Srdjan S; Dale, Anders M AM
Publication Date: 2013-04

Variant appearance in text: rs10277665
PubMed Link: 23637625
Variant Present in the following documents:
  • Main text
  • pgen.1003455.pdf
View BVdb publication page