MYBL2 c.1506-1919C>A

Variant ID: 20-42336684-C-A

NM_002466.3(MYBL2):c.1506-1919C>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


MYBL2 alternative splicing-related genetic variants reduce the risk of triple-negative breast cancer in the Chinese population.

Frontiers In Genetics
Chen, Xinyu X; Feng, Jin J; Zhang, Yuan Y; Liu, Jiarui J; Zhang, Lijia L; Zeng, Pu P; Wen, Langbo L; Wang, Xin X; Zhang, Yi Y
Publication Date: 2023

Variant appearance in text: rs420755
PubMed Link: 37144133
Variant Present in the following documents:
  • DataSheet2.xlsx, sheet 1
View BVdb publication page



Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs420755
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page