SMAD4 c.956-2075T>C

Variant ID: 18-48589718-T-C

NM_005359.5(SMAD4):c.956-2075T>C

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Associations of SMAD4 rs10502913 and NLRP3 rs1539019 Polymorphisms with Risk of Coal Workers' Pneumoconiosis Susceptibility in Chinese Han Population.

Pharmacogenomics And Personalized Medicine
Zhao, Hai H; Huang, Yaqiong Y; Wang, Hao H; Zhao, Juan J; Tian, Shanshan S; Bai, Haixia H; Guo, Mufang M; Dong, Caiping C; Shi, Yongliang Y; Li, Xia X; Zhu, Chengjun C; Feng, Tao T; Ma, Xia X; Hou, Zhifei Z
Publication Date: 2022

Variant appearance in text: rs17663887
PubMed Link: 35280939
Variant Present in the following documents:
  • Main text
  • pgpm-15-167.pdf
View BVdb publication page



Genetic susceptibility to chronic otitis media with effusion: candidate gene single nucleotide polymorphisms.

The Laryngoscope
MacArthur, Carol J CJ; Wilmot, Beth B; Wang, Linda L; Schuller, Michael M; Lighthall, Jessyka J; Trune, Dennis D
Publication Date: 2014-05

Variant appearance in text: rs17663887
PubMed Link: 23929584
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variations in the SMAD4 gene and gastric cancer susceptibility.

World Journal Of Gastroenterology
Wu, Dong-Mei DM; Zhu, Hai-Xia HX; Zhao, Qing-Hong QH; Zhang, Zhi-Zhong ZZ; Wang, Shi-Zhi SZ; Wang, Mei-Lin ML; Gong, Wei-Da WD; Tan, Ming M; Zhang, Zheng-Dong ZD
Publication Date: 2010-11-28

Variant appearance in text: rs17663887
PubMed Link: 21105199
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance.

American Journal Of Human Genetics
Milet, Jacqueline J; Dehais, Valerie V; Bourgain, Catherine C; Jouanolle, Anne Marie AM; Mosser, Annick A; Perrin, Michele M; Morcet, Jeff J; Brissot, Pierre P; David, Veronique V; Deugnier, Yves Y; Mosser, Jean J
Publication Date: 2007-10

Variant appearance in text: rs17663887
PubMed Link: 17847004
Variant Present in the following documents:
  • Main text
View BVdb publication page