RELN c.226+1542G>A

Variant ID: 7-103628036-C-T

NM_005045.3(RELN):c.226+1542G>A

This variant was identified in 20 publications

View GRCh38 version.




Publications:


Genome-wide association testing in malaria studies in the presence of overdominance.

Malaria Journal
Akoth, Morine M; Odhiambo, John J; Omolo, Bernard B
Publication Date: 2023-04-10

Variant appearance in text: rs17157903
PubMed Link: 37038187
Variant Present in the following documents:
  • Main text
  • 12936_2023_Article_4533.pdf
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Delineation of the Germline and Somatic Mutation Interaction Landscape in Triple-Negative and Non-Triple-Negative Breast Cancer.

International Journal Of Genomics
Wu, Jiande J; Mamidi, Tarun K K TKK; Zhang, Lu L; Hicks, Chindo C
Publication Date: 2020

Variant appearance in text: rs17157903
PubMed Link: 32724790
Variant Present in the following documents:
  • Main text
  • IJG2020-2641370.pdf
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Replication analysis of variants associated with multiple sclerosis risk.

Scientific Reports
Dashti, Mohammad M; Ateyah, Khadijah K; Alroughani, Raed R; Al-Temaimi, Rabeah R
Publication Date: 2020-04-30

Variant appearance in text: rs17157903
PubMed Link: 32355262
Variant Present in the following documents:
  • 41598_2020_64432_MOESM1_ESM.pdf
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Deconvolution of the Genomic and Epigenomic Interaction Landscape of Triple-Negative Breast Cancer.

Cancers
Wu, Jiande J; Mamidi, Tarun Karthik Kumar TKK; Zhang, Lu L; Hicks, Chindo C
Publication Date: 2019-10-31

Variant appearance in text: rs17157903
PubMed Link: 31683572
Variant Present in the following documents:
  • Main text
  • cancers-11-01692.pdf
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Integrating Germline and Somatic Mutation Information for the Discovery of Biomarkers in Triple-Negative Breast Cancer.

International Journal Of Environmental Research And Public Health
Wu, Jiande J; Mamidi, Tarun Karthik Kumar TKK; Zhang, Lu L; Hicks, Chindo C
Publication Date: 2019-03-23

Variant appearance in text: rs17157903
PubMed Link: 30909550
Variant Present in the following documents:
  • Main text
  • ijerph-16-01055.pdf
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Interaction between common breast cancer susceptibility variants, genetic ancestry, and nongenetic risk factors in Hispanic women.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Fejerman, Laura L; Stern, Mariana C MC; John, Esther M EM; Torres-Mejía, Gabriela G; Hines, Lisa M LM; Wolff, Roger K RK; Baumgartner, Kathy B KB; Giuliano, Anna R AR; Ziv, Elad E; Pérez-Stable, Eliseo J EJ; Slattery, Martha L ML
Publication Date: 2015-11

Variant appearance in text: rs17157903
PubMed Link: 26364163
Variant Present in the following documents:
  • Main text
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LEAP: biomarker inference through learning and evaluating association patterns.

Genetic Epidemiology
Jiang, Xia X; Neapolitan, Richard E RE
Publication Date: 2015-03

Variant appearance in text: rs17157903
PubMed Link: 25677188
Variant Present in the following documents:
  • Main text
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Breast cancer prediction using genome wide single nucleotide polymorphism data.

Bmc Bioinformatics
Hajiloo, Mohsen M; Damavandi, Babak B; Hooshsadat, Metanat M; Sangi, Farzad F; Mackey, John R JR; Cass, Carol E CE; Greiner, Russell R; Damaraju, Sambasivarao S
Publication Date: 2013

Variant appearance in text: rs17157903
PubMed Link: 24266904
Variant Present in the following documents:
  • Main text
  • 1471-2105-14-S13-S3.pdf
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Replication of breast cancer susceptibility loci in whites and African Americans using a Bayesian approach.

American Journal Of Epidemiology
O'Brien, Katie M KM; Cole, Stephen R SR; Poole, Charles C; Bensen, Jeannette T JT; Herring, Amy H AH; Engel, Lawrence S LS; Millikan, Robert C RC
Publication Date: 2014-02-01

Variant appearance in text: rs17157903
PubMed Link: 24218030
Variant Present in the following documents:
  • Main text
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Breast cancer subtypes and previously established genetic risk factors: a bayesian approach.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
O'Brien, Katie M KM; Cole, Stephen R SR; Engel, Lawrence S LS; Bensen, Jeannette T JT; Poole, Charles C; Herring, Amy H AH; Millikan, Robert C RC
Publication Date: 2014-01

Variant appearance in text: rs17157903
PubMed Link: 24177593
Variant Present in the following documents:
  • Main text
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Novel Integrative Genomics Approach for Associating GWAS Information with Intrinsic Subtypes of Breast Cancer.

Cancer Informatics
Hicks, Chindo C; Koganti, Tejaswi T; Brown, Alexandra S AS; Monico, Jesus J; Backus, Kandis K; Miele, Lucio L
Publication Date: 2013

Variant appearance in text: rs17157903
PubMed Link: 23761956
Variant Present in the following documents:
  • Main text
  • cin-12-2013-125.pdf
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Genetic ancestry modifies the association between genetic risk variants and breast cancer risk among Hispanic and non-Hispanic white women.

Carcinogenesis
Fejerman, Laura L; Stern, Mariana C MC; Ziv, Elad E; John, Esther M EM; Torres-Mejia, Gabriela G; Hines, Lisa M LM; Wolff, Roger R; Wang, Wei W; Baumgartner, Kathy B KB; Giuliano, Anna R AR; Slattery, Martha L ML
Publication Date: 2013-08

Variant appearance in text: rs17157903
PubMed Link: 23563089
Variant Present in the following documents:
  • Main text
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Integrative Analysis of Response to Tamoxifen Treatment in ER-Positive Breast Cancer Using GWAS Information and Transcription Profiling.

Breast Cancer : Basic And Clinical Research
Hicks, Chindo C; Kumar, Ranjit R; Pannuti, Antonio A; Miele, Lucio L
Publication Date: 2012

Variant appearance in text: rs17157903
PubMed Link: 22399860
Variant Present in the following documents:
  • Main text
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A robust method for testing association in genome-wide association studies.

Human Heredity
Chen, Zhongxue Z; Ng, Hon Keung Tony HK
Publication Date: 2012

Variant appearance in text: rs17157903
PubMed Link: 22212363
Variant Present in the following documents:
  • Main text
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A bayesian method for evaluating and discovering disease loci associations.

Plos One
Jiang, Xia X; Barmada, M Michael MM; Cooper, Gregory F GF; Becich, Michael J MJ
Publication Date: 2011

Variant appearance in text: rs17157903
PubMed Link: 21853025
Variant Present in the following documents:
  • Main text
  • pone.0022075.pdf
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Powerful SNP-set analysis for case-control genome-wide association studies.

American Journal Of Human Genetics
Wu, Michael C MC; Kraft, Peter P; Epstein, Michael P MP; Taylor, Deanne M DM; Chanock, Stephen J SJ; Hunter, David J DJ; Lin, Xihong X
Publication Date: 2010-06-11

Variant appearance in text: rs17157903
PubMed Link: 20560208
Variant Present in the following documents:
  • Main text
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FGFR2 and other loci identified in genome-wide association studies are associated with breast cancer in African-American and younger women.

Carcinogenesis
Barnholtz-Sloan, Jill S JS; Shetty, Priya B PB; Guan, Xiaowei X; Nyante, Sarah J SJ; Luo, Jingchun J; Brennan, Donal J DJ; Millikan, Robert C RC
Publication Date: 2010-08

Variant appearance in text: rs17157903
PubMed Link: 20554749
Variant Present in the following documents:
  • Main text
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Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.

Genetic Epidemiology
Zhong, Hua H; Prentice, Ross L RL
Publication Date: 2010-01

Variant appearance in text: rs17157903
PubMed Link: 19639606
Variant Present in the following documents:
  • Main text
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Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.

Human Molecular Genetics
Baranzini, Sergio E SE; Wang, Joanne J; Gibson, Rachel A RA; Galwey, Nicholas N; Naegelin, Yvonne Y; Barkhof, Frederik F; Radue, Ernst-Wilhelm EW; Lindberg, Raija L P RL; Uitdehaag, Bernard M G BM; Johnson, Michael R MR; Angelakopoulou, Aspasia A; Hall, Leslie L; Richardson, Jill C JC; Prinjha, Rab K RK; Gass, Achim A; Geurts, Jeroen J G JJ; Kragt, Jolijn J; Sombekke, Madeleine M; Vrenken, Hugo H; Qualley, Pamela P; Lincoln, Robin R RR; Gomez, Refujia R; Caillier, Stacy J SJ; George, Michaela F MF; Mousavi, Hourieh H; Guerrero, Rosa R; Okuda, Darin T DT; Cree, Bruce A C BA; Green, Ari J AJ; Waubant, Emmanuelle E; Goodin, Douglas S DS; Pelletier, Daniel D; Matthews, Paul M PM; Hauser, Stephen L SL; Kappos, Ludwig L; Polman, Chris H CH; Oksenberg, Jorge R JR
Publication Date: 2009-02-15

Variant appearance in text: rs17157903
PubMed Link: 19010793
Variant Present in the following documents:
  • Main text
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A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.

Nature Genetics
Hunter, David J DJ; Kraft, Peter P; Jacobs, Kevin B KB; Cox, David G DG; Yeager, Meredith M; Hankinson, Susan E SE; Wacholder, Sholom S; Wang, Zhaoming Z; Welch, Robert R; Hutchinson, Amy A; Wang, Junwen J; Yu, Kai K; Chatterjee, Nilanjan N; Orr, Nick N; Willett, Walter C WC; Colditz, Graham A GA; Ziegler, Regina G RG; Berg, Christine D CD; Buys, Saundra S SS; McCarty, Catherine A CA; Feigelson, Heather Spencer HS; Calle, Eugenia E EE; Thun, Michael J MJ; Hayes, Richard B RB; Tucker, Margaret M; Gerhard, Daniela S DS; Fraumeni, Joseph F JF; Hoover, Robert N RN; Thomas, Gilles G; Chanock, Stephen J SJ
Publication Date: 2007-07

Variant appearance in text: rs17157903
PubMed Link: 17529973
Variant Present in the following documents:
  • Main text
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