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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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