IKZF1 c.850+535G>A

Variant ID: 7-50460096-G-A

NM_006060.6(IKZF1):c.850+535G>A

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Association of IKZF1 and CDKN2A gene polymorphisms with childhood acute lymphoblastic leukemia: a high-resolution melting analysis.

Bmc Medical Genomics
Sattarzadeh Bardsiri, Mahla M; Zehtab, Shahrzad S; Karami, Najibe N; Farsinejad, Alireza A; Ehsan, Mohsen M; Fatemi, Ahmad A
Publication Date: 2022-08-05

Variant appearance in text: rs6964823
PubMed Link: 35932035
Variant Present in the following documents:
  • Main text
  • 12920_2022_Article_1325.pdf
View BVdb publication page



Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs6964823
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



IKZF1 genetic variants rs4132601 and rs11978267 and acute lymphoblastic leukemia risk in Tunisian children: a case-control study.

Bmc Medical Genetics
Mahjoub, Sana S; Chayeb, Vera V; Zitouni, Hedia H; Ghali, Rabeb M RM; Regaieg, Haifa H; Almawi, Wassim Y WY; Mahjoub, Touhami T
Publication Date: 2019-10-11

Variant appearance in text: rs6964823
PubMed Link: 31604453
Variant Present in the following documents:
  • Main text
  • 12881_2019_Article_900.pdf
View BVdb publication page



Family-based exome-wide association study of childhood acute lymphoblastic leukemia among Hispanics confirms role of ARID5B in susceptibility.

Plos One
Archer, Natalie P NP; Perez-Andreu, Virginia V; Stoltze, Ulrik U; Scheurer, Michael E ME; Wilkinson, Anna V AV; Lin, Ting-Nien TN; Qian, Maoxiang M; Goodings, Charnise C; Swartz, Michael D MD; Ranjit, Nalini N; Rabin, Karen R KR; Peckham-Gregory, Erin C EC; Plon, Sharon E SE; de Alarcon, Pedro A PA; Zabriskie, Ryan C RC; Antillon-Klussmann, Federico F; Najera, Cesar R CR; Yang, Jun J JJ; Lupo, Philip J PJ
Publication Date: 2017

Variant appearance in text: rs6964823
PubMed Link: 28817678
Variant Present in the following documents:
  • Main text
  • pone.0180488.pdf
View BVdb publication page



Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes.

Bmc Cancer
Spinella, Jean-François JF; Healy, Jasmine J; Saillour, Virginie V; Richer, Chantal C; Cassart, Pauline P; Ouimet, Manon M; Sinnett, Daniel D
Publication Date: 2015-07-23

Variant appearance in text: rs6964823
PubMed Link: 26201965
Variant Present in the following documents:
  • Main text
  • 12885_2015_Article_1549.pdf
View BVdb publication page



USP38, FREM3, SDC1, DDC, and LOC727982 Gene Polymorphisms and Differential Susceptibility to Severe Malaria in Tanzania.

The Journal Of Infectious Diseases
Manjurano, Alphaxard A; Sepúlveda, Nuno N; Nadjm, Behzad B; Mtove, George G; Wangai, Hannah H; Maxwell, Caroline C; Olomi, Raimos R; Reyburn, Hugh H; Drakeley, Christopher J CJ; Riley, Eleanor M EM; Clark, Taane G TG; ,
Publication Date: 2015-10-01

Variant appearance in text: rs6964823
PubMed Link: 25805752
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children.

Cancer Causes & Control : Ccc
Hsu, Ling-I LI; Chokkalingam, Anand P AP; Briggs, Farren B S FB; Walsh, Kyle K; Crouse, Vonda V; Fu, Cecilia C; Metayer, Catherine C; Wiemels, Joseph L JL; Barcellos, Lisa F LF; Buffler, Patricia A PA
Publication Date: 2015-04

Variant appearance in text: rs6964823
PubMed Link: 25761407
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.

Leukemia
Ellinghaus, E E; Stanulla, M M; Richter, G G; Ellinghaus, D D; te Kronnie, G G; Cario, G G; Cazzaniga, G G; Horstmann, M M; Panzer Grümayer, R R; Cavé, H H; Trka, J J; Cinek, O O; Teigler-Schlegel, A A; ElSharawy, A A; Häsler, R R; Nebel, A A; Meissner, B B; Bartram, T T; Lescai, F F; Franceschi, C C; Giordan, M M; Nürnberg, P P; Heinzow, B B; Zimmermann, M M; Schreiber, S S; Schrappe, M M; Franke, A A
Publication Date: 2012-05

Variant appearance in text: rs6964823
PubMed Link: 22076464
Variant Present in the following documents:
  • leu2011302a.pdf
View BVdb publication page



Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.

Nature Genetics
Papaemmanuil, Elli E; Hosking, Fay J FJ; Vijayakrishnan, Jayaram J; Price, Amy A; Olver, Bianca B; Sheridan, Eammon E; Kinsey, Sally E SE; Lightfoot, Tracy T; Roman, Eve E; Irving, Julie A E JA; Allan, James M JM; Tomlinson, Ian P IP; Taylor, Malcolm M; Greaves, Mel M; Houlston, Richard S RS
Publication Date: 2009-09

Variant appearance in text: rs6964823
PubMed Link: 19684604
Variant Present in the following documents:
  • Main text
  • emss-27409.pdf
View BVdb publication page