CSMD1 c.415+86682G>T

Variant ID: 8-4190793-C-A

NM_033225.5(CSMD1):c.415+86682G>T

This variant was identified in 7 publications

View GRCh38 version.




Publications:


New Insight into the human genetic diversity in North African populations by genotyping of SNPs in DRD3, CSMD1 and NRG1 genes.

Molecular Genetics & Genomic Medicine
Mestiri, Souhir S; Boussetta, Sami S; Pakstis, Andrew J AJ; El Kamel, Sarra S; Ben Ammar El Gaaied, Amel A; Kidd, Kenneth K KK; Cherni, Lotfi L
Publication Date: 2022-03

Variant appearance in text: rs10108270
PubMed Link: 35128830
Variant Present in the following documents:
  • Main text
  • MGG3-10-e1871.pdf
View BVdb publication page



Pushing the Boundaries: Forensic DNA Phenotyping Challenged by Single-Cell Sequencing.

Genes
Diepenbroek, Marta M; Bayer, Birgit B; Anslinger, Katja K
Publication Date: 2021-08-30

Variant appearance in text: rs10108270
PubMed Link: 34573344
Variant Present in the following documents:
  • genes-12-01362.pdf
View BVdb publication page



DCDC2 READ1 regulatory element: how temporal processing differences may shape language.

Proceedings. Biological Sciences
Tang, Kevin K; DeMille, Mellissa M C MMC; Frijters, Jan C JC; Gruen, Jeffrey R JR
Publication Date: 2020-06-10

Variant appearance in text: rs10108270
PubMed Link: 32486976
Variant Present in the following documents:
  • rspb20192712supp1.pdf
View BVdb publication page



Data on a genome-wide association study of type 2 diabetes in a Maya population.

Data In Brief
Totomoch-Serra, Armando A; Domínguez-Cruz, Miriam Givisay MG; Muñoz, María de Lourdes ML; García-Escalante, María Guadalupe MG; Burgueño, Juan J; Díaz-Badillo, Álvaro Á; Valadez-González, Nina N; Escalante, Doris Pinto DP
Publication Date: 2020-02

Variant appearance in text: rs10108270
PubMed Link: 31872004
Variant Present in the following documents:
  • Main text
View BVdb publication page



Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes.

Journal Of Thrombosis And Haemostasis : Jth
de Haan, H G HG; van Hylckama Vlieg, A A; Lotta, L A LA; Gorski, M M MM; Bucciarelli, P P; Martinelli, I I; Baglin, T P TP; Peyvandi, F F; Rosendaal, F R FR; ,
Publication Date: 2018-12

Variant appearance in text: rs10108270
PubMed Link: 30168256
Variant Present in the following documents:
  • NIHMS1021906-supplement-1.pdf
View BVdb publication page



The 22Rv1 prostate cancer cell line carries mixed genetic ancestry: Implications for prostate cancer health disparities research using pre-clinical models.

The Prostate
Woods-Burnham, Leanne L; Basu, Anamika A; Cajigas-Du Ross, Christina K CK; Love, Arthur A; Yates, Clayton C; De Leon, Marino M; Roy, Sourav S; Casiano, Carlos A CA
Publication Date: 2017-12

Variant appearance in text: rs10108270
PubMed Link: 29030865
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic susceptibility to therapy-related leukemia after Hodgkin lymphoma or non-Hodgkin lymphoma: role of drug metabolism, apoptosis and DNA repair.

Blood Cancer Journal
Ding, Y Y; Sun, C-L CL; Li, L L; Li, M M; Francisco, L L; Sabado, M M; Hahn, B B; Gyorffy, J J; Noe, J J; Larson, G P GP; Forman, S J SJ; Bhatia, R R; Bhatia, S S
Publication Date: 2012-03

Variant appearance in text: rs10108270
PubMed Link: 22829253
Variant Present in the following documents:
View BVdb publication page