MSH2 c.2635-765G>A

Variant ID: 2-47709153-G-A

NM_000251.2(MSH2):c.2635-765G>A

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Systematic Review of Genetic Factors in the Etiology of Esophageal Squamous Cell Carcinoma in African Populations.

Frontiers In Genetics
Simba, Hannah H; Kuivaniemi, Helena H; Lutje, Vittoria V; Tromp, Gerard G; Sewram, Vikash V
Publication Date: 2019

Variant appearance in text: rs10188090
PubMed Link: 31428123
Variant Present in the following documents:
  • Main text
  • fgene-10-00642.pdf
View BVdb publication page



Genetic Polymorphisms of DNA Repair Pathways in Sporadic Colorectal Carcinogenesis.

Journal Of Cancer
Liu, Jingwei J; Zheng, Bowen B; Li, Ying Y; Yuan, Yuan Y; Xing, Chengzhong C
Publication Date: 2019

Variant appearance in text: rs10188090
PubMed Link: 31031852
Variant Present in the following documents:
  • Main text
  • jcav10p1417.pdf
View BVdb publication page



DNA methylation mapping identifies gene regulatory effects in patients with systemic lupus erythematosus.

Annals Of The Rheumatic Diseases
Imgenberg-Kreuz, Juliana J; Carlsson Almlöf, Jonas J; Leonard, Dag D; Alexsson, Andrei A; Nordmark, Gunnel G; Eloranta, Maija-Leena ML; Rantapää-Dahlqvist, Solbritt S; Bengtsson, Anders A AA; Jönsen, Andreas A; Padyukov, Leonid L; Gunnarsson, Iva I; Svenungsson, Elisabet E; Sjöwall, Christopher C; Rönnblom, Lars L; Syvänen, Ann-Christine AC; Sandling, Johanna K JK
Publication Date: 2018-05

Variant appearance in text: rs10188090
PubMed Link: 29437559
Variant Present in the following documents:
  • annrheumdis-2017-212379supp016.pdf
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs10188090
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



DNA repair genotype and lung cancer risk in the beta-carotene and retinol efficacy trial.

International Journal Of Molecular Epidemiology And Genetics
Doherty, Jennifer A JA; Sakoda, Lori C LC; Loomis, Melissa M MM; Barnett, Matt J MJ; Julianto, Liberto L; Thornquist, Mark D MD; Neuhouser, Marian L ML; Weiss, Noel S NS; Goodman, Gary E GE; Chen, Chu C
Publication Date: 2013

Variant appearance in text: rs10188090
PubMed Link: 23565320
Variant Present in the following documents:
  • Main text
View BVdb publication page



The cumulative effects of polymorphisms in the DNA mismatch repair genes and tobacco smoking in oesophageal cancer risk.

Plos One
Vogelsang, Matjaz M; Wang, Yabing Y; Veber, Nika N; Mwapagha, Lamech M LM; Parker, M Iqbal MI
Publication Date: 2012

Variant appearance in text: rs10188090
PubMed Link: 22623965
Variant Present in the following documents:
  • Main text
  • pone.0036962.pdf
  • pone.0036962.s002.pdf
View BVdb publication page



SNP-SNP interactions between dNTP supply enzymes and mismatch DNA repair in breast cancer.

Proceedings. Ohio Collaborative Conference On Bioinformatics
Feng, I Jung IJ; Radivoyevitch, Tomas T
Publication Date: 2009-06-15

Variant appearance in text: rs10188090
PubMed Link: 21566726
Variant Present in the following documents:
  • Main text
View BVdb publication page