MBD2 c.1109+1938G>A

Variant ID: 18-51688955-C-T

NM_003927.4(MBD2):c.1109+1938G>A

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs1145315
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



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: rs1145315
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Identification of six polymorphisms as novel susceptibility loci for ischemic or hemorrhagic stroke by exome-wide association studies.

International Journal Of Molecular Medicine
Yamada, Yoshiji Y; Sakuma, Jun J; Takeuchi, Ichiro I; Yasukochi, Yoshiki Y; Kato, Kimihiko K; Oguri, Mitsutoshi M; Fujimaki, Tetsuo T; Horibe, Hideki H; Muramatsu, Masaaki M; Sawabe, Motoji M; Fujiwara, Yoshinori Y; Taniguchi, Yu Y; Obuchi, Shuichi S; Kawai, Hisashi H; Shinkai, Shoji S; Mori, Seijiro S; Arai, Tomio T; Tanaka, Masashi M
Publication Date: 2017-06

Variant appearance in text: rs1145315
PubMed Link: 28487959
Variant Present in the following documents:
  • Main text
  • ijmm-39-06-1477.pdf
View BVdb publication page



Detecting gene-gene interactions using a permutation-based random forest method.

Biodata Mining
Li, Jing J; Malley, James D JD; Andrew, Angeline S AS; Karagas, Margaret R MR; Moore, Jason H JH
Publication Date: 2016

Variant appearance in text: rs1145315
PubMed Link: 27053949
Variant Present in the following documents:
  • Main text
  • 13040_2016_Article_93.pdf
View BVdb publication page



Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy.

Plos One
Li, Yi-Ju YJ; Minear, Mollie A MA; Rimmler, Jacqueline J; Zhao, Bei B; Balajonda, Elmer E; Hauser, Michael A MA; Allingham, R Rand RR; Eghrari, Allen O AO; Riazuddin, S Amer SA; Katsanis, Nicholas N; Gottsch, John D JD; Gregory, Simon G SG; Klintworth, Gordon K GK; Afshari, Natalie A NA
Publication Date: 2011-04-20

Variant appearance in text: rs1145315
PubMed Link: 21533127
Variant Present in the following documents:
  • Main text
  • pone.0018044.pdf
View BVdb publication page



Genome-wide linkage analyses of hereditary prostate cancer families with colon cancer provide further evidence for a susceptibility locus on 15q11-q14.

European Journal Of Human Genetics : Ejhg
Fitzgerald, Liesel M LM; McDonnell, Shannon K SK; Carlson, Erin E EE; Langeberg, Wendy W; McIntosh, Laura M LM; Deutsch, Kerry K; Ostrander, Elaine A EA; Schaid, Daniel J DJ; Stanford, Janet L JL
Publication Date: 2010-10

Variant appearance in text: rs1145315
PubMed Link: 20407467
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic analysis of diabetic nephropathy on chromosome 18 in African Americans: linkage analysis and dense SNP mapping.

Human Genetics
McDonough, Caitrin W CW; Bostrom, Meredith A MA; Lu, Lingyi L; Hicks, Pamela J PJ; Langefeld, Carl D CD; Divers, Jasmin J; Mychaleckyj, Josyf C JC; Freedman, Barry I BI; Bowden, Donald W DW
Publication Date: 2009-12

Variant appearance in text: rs1145315
PubMed Link: 19690890
Variant Present in the following documents:
  • Main text
View BVdb publication page



Dense genome-wide SNP linkage scan in 301 hereditary prostate cancer families identifies multiple regions with suggestive evidence for linkage.

Human Molecular Genetics
Stanford, Janet L JL; FitzGerald, Liesel M LM; McDonnell, Shannon K SK; Carlson, Erin E EE; McIntosh, Laura M LM; Deutsch, Kerry K; Hood, Lee L; Ostrander, Elaine A EA; Schaid, Daniel J DJ
Publication Date: 2009-05-15

Variant appearance in text: rs1145315
PubMed Link: 19251732
Variant Present in the following documents:
  • Main text
View BVdb publication page