CUX2 c.2003-3219T>C

Variant ID: 12-111754597-T-C

NM_015267.3(CUX2):c.2003-3219T>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Multiple genotype-phenotype association study reveals intronic variant pair on SIDT2 associated with metabolic syndrome in a Korean population.

Human Genomics
Moon, Sanghoon S; Lee, Young Y; Won, Sungho S; Lee, Juyoung J
Publication Date: 2018-11-01

Variant appearance in text: rs7300860
PubMed Link: 30382898
Variant Present in the following documents:
  • Main text
View BVdb publication page



Uncovering the complex genetics of human character.

Molecular Psychiatry
Zwir, Igor I; Arnedo, Javier J; Del-Val, Coral C; Pulkki-Råback, Laura L; Konte, Bettina B; Yang, Sarah S SS; Romero-Zaliz, Rocio R; Hintsanen, Mirka M; Cloninger, Kevin M KM; Garcia, Danilo D; Svrakic, Dragan M DM; Rozsa, Sandor S; Martinez, Maribel M; Lyytikäinen, Leo-Pekka LP; Giegling, Ina I; Kähönen, Mika M; Hernandez-Cuervo, Helena H; Seppälä, Ilkka I; Raitoharju, Emma E; de Erausquin, Gabriel A GA; Raitakari, Olli O; Rujescu, Dan D; Postolache, Teodor T TT; Sung, Joohon J; Keltikangas-Järvinen, Liisa L; Lehtimäki, Terho T; Cloninger, C Robert CR
Publication Date: 2020-10

Variant appearance in text: CUX2: 2003-3219T>C; rs7300860
PubMed Link: 30283034
Variant Present in the following documents:
  • 41380_2018_263_MOESM14_ESM.xlsx, sheet 1
View BVdb publication page



Uncovering the complex genetics of human temperament.

Molecular Psychiatry
Zwir, Igor I; Arnedo, Javier J; Del-Val, Coral C; Pulkki-Råback, Laura L; Konte, Bettina B; Yang, Sarah S SS; Romero-Zaliz, Rocio R; Hintsanen, Mirka M; Cloninger, Kevin M KM; Garcia, Danilo D; Svrakic, Dragan M DM; Rozsa, Sandor S; Martinez, Maribel M; Lyytikäinen, Leo-Pekka LP; Giegling, Ina I; Kähönen, Mika M; Hernandez-Cuervo, Helena H; Seppälä, Ilkka I; Raitoharju, Emma E; de Erausquin, Gabriel A GA; Raitakari, Olli O; Rujescu, Dan D; Postolache, Teodor T TT; Sung, Joohon J; Keltikangas-Järvinen, Liisa L; Lehtimäki, Terho T; Cloninger, C Robert CR
Publication Date: 2020-10

Variant appearance in text: CUX2: 2003-3219T>C; rs7300860
PubMed Link: 30279457
Variant Present in the following documents:
  • 41380_2018_264_MOESM15_ESM.xlsx, sheet 1
View BVdb publication page