SMAD7 c.742+5899A>G

Variant ID: 18-46462952-T-C

NM_005904.3(SMAD7):c.742+5899A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


The association of low penetrance genetic risk modifiers with colorectal cancer in lynch syndrome patients: a systematic review and meta-analysis.

Familial Cancer
Donald, Neil N; Malik, Salim S; McGuire, Joshua L JL; Monahan, Kevin J KJ
Publication Date: 2018-01

Variant appearance in text: rs2337104
PubMed Link: 28508326
Variant Present in the following documents:
  • 10689_2017_Article_9995.pdf
View BVdb publication page



Polymorphism of SMAD7 gene (rs2337104) and risk of colorectal cancer in an Iranian population: a case-control study.

Gastroenterology And Hepatology From Bed To Bench
Akbari, Zahra Z; Safari-Alighiarloo, Nahid N; Taleghani, Mohammad Yaghoob MY; Mirfakhar, Farzaneh Sadat FS; Asadzadeh Aghdaei, Hamid H; Vahedi, Mohsen M; Irani Shemirani, Atena A; Nazemalhosseini-Mojarad, Ehsan E; Zali, Mohammad Reza MR
Publication Date: 2014

Variant appearance in text: rs2337104
PubMed Link: 25289133
Variant Present in the following documents:
  • Main text
  • GHFBB-7-198.pdf
View BVdb publication page



A large-scale candidate gene association study of age at menarche and age at natural menopause.

Human Genetics
He, Chunyan C; Kraft, Peter P; Chasman, Daniel I DI; Buring, Julie E JE; Chen, Constance C; Hankinson, Susan E SE; Paré, Guillaume G; Chanock, Stephen S; Ridker, Paul M PM; Hunter, David J DJ
Publication Date: 2010-11

Variant appearance in text: rs2337104
PubMed Link: 20734064
Variant Present in the following documents:
  • Main text
View BVdb publication page