NCOA3 c.3253-1632G>A

Variant ID: 20-46274185-G-A

NM_181659.2(NCOA3):c.3253-1632G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: rs427967
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



NFE2L2 pathway polymorphisms and lung function decline in chronic obstructive pulmonary disease.

Physiological Genomics
Sandford, Andrew J AJ; Malhotra, Deepti D; Boezen, H Marike HM; Siedlinski, Mateusz M; Postma, Dirkje S DS; Wong, Vivien V; Akhabir, Loubna L; He, Jian-Qing JQ; Connett, John E JE; Anthonisen, Nicholas R NR; Paré, Peter D PD; Biswal, Shyam S
Publication Date: 2012-08-01

Variant appearance in text: rs427967
PubMed Link: 22693272
Variant Present in the following documents:
  • Main text
View BVdb publication page