ERBB2 c.74-1525T>G

Variant ID: 17-37861718-T-G

NM_004448.2(ERBB2):c.74-1525T>G

This variant was identified in 14 publications

View GRCh38 version.




Publications:


Pharmacogenomics deliberations of 2-deoxy-d-glucose in the treatment of COVID-19 disease: an in silico approach.

3 Biotech
Prabhu, Navya B NB; Vinay, Chigateri M CM; Satyamoorthy, Kapaettu K; Rai, Padmalatha S PS
Publication Date: 2022-11

Variant appearance in text: rs2952155
PubMed Link: 36164436
Variant Present in the following documents:
  • Main text
  • 13205_2022_Article_3363.pdf
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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: rs2952155
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
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An association analysis to identify genetic variants linked to asthma and rhino-conjunctivitis in a cohort of Sicilian children.

Italian Journal Of Pediatrics
Sottile, Gianluca G; Ferrante, Giuliana G; Torregrossa, Marta M; Cibella, Fabio F; Cilluffo, Giovanna G; Fasola, Salvatore S; Alessandro, Riccardo R; Seidita, Gregorio G; Viegi, Giovanni G; La Grutta, Stefania S
Publication Date: 2019-01-15

Variant appearance in text: rs2952155
PubMed Link: 30646946
Variant Present in the following documents:
  • Main text
  • 13052_2019_Article_603.pdf
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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs2952155
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Detection and interpretation of shared genetic influences on 42 human traits.

Nature Genetics
Pickrell, Joseph K JK; Berisa, Tomaz T; Liu, Jimmy Z JZ; Ségurel, Laure L; Tung, Joyce Y JY; Hinds, David A DA
Publication Date: 2016-07

Variant appearance in text: rs2952155
PubMed Link: 27182965
Variant Present in the following documents:
  • NIHMS780506-supplement-5.pdf
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Single nucleotide polymorphisms of HER2 related to osteosarcoma susceptibility.

International Journal Of Clinical And Experimental Pathology
Xin, Da-Jiang DJ; Shen, Guo-Dong GD; Song, Jian J
Publication Date: 2015

Variant appearance in text: rs2952155
PubMed Link: 26464710
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of difference of association between polymorphisms in the XRCC5, RPA3 and RTEL1 genes and glioma, astrocytoma and glioblastoma.

American Journal Of Cancer Research
Jin, Tianbo T; Wang, Yuan Y; Li, Gang G; Du, Shuli S; Yang, Hua H; Geng, Tingting T; Hou, Peng P; Gong, Yongkuan Y
Publication Date: 2015

Variant appearance in text: rs2952155
PubMed Link: 26328260
Variant Present in the following documents:
  • Main text
View BVdb publication page



EGFR gene variants are associated with specific somatic aberrations in glioma.

Plos One
Wibom, Carl C; Ghasimi, Soma S; Van Loo, Peter P; Brännström, Thomas T; Trygg, Johan J; Lau, Ching C; Henriksson, Roger R; Bergenheim, Tommy T; Andersson, Ulrika U; Rydén, Patrik P; Melin, Beatrice B
Publication Date: 2012

Variant appearance in text: rs2952155
PubMed Link: 23236348
Variant Present in the following documents:
  • Main text
  • pone.0047929.pdf
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Examination of the relationship between variation at 17q21 and childhood wheeze phenotypes.

The Journal Of Allergy And Clinical Immunology
Granell, Raquel R; Henderson, A John AJ; Timpson, Nicholas N; St Pourcain, Beate B; Kemp, John P JP; Ring, Susan M SM; Ho, Karen K; Montgomery, Stephen B SB; Dermitzakis, Emmanouil T ET; Evans, David M DM; Sterne, Jonathan A C JA
Publication Date: 2013-03

Variant appearance in text: rs2952155
PubMed Link: 23154084
Variant Present in the following documents:
  • Main text
View BVdb publication page



Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations.

Nature Genetics
Torgerson, Dara G DG; Ampleford, Elizabeth J EJ; Chiu, Grace Y GY; Gauderman, W James WJ; Gignoux, Christopher R CR; Graves, Penelope E PE; Himes, Blanca E BE; Levin, Albert M AM; Mathias, Rasika A RA; Hancock, Dana B DB; Baurley, James W JW; Eng, Celeste C; Stern, Debra A DA; Celedón, Juan C JC; Rafaels, Nicholas N; Capurso, Daniel D; Conti, David V DV; Roth, Lindsey A LA; Soto-Quiros, Manuel M; Togias, Alkis A; Li, Xingnan X; Myers, Rachel A RA; Romieu, Isabelle I; Van Den Berg, David J DJ; Hu, Donglei D; Hansel, Nadia N NN; Hernandez, Ryan D RD; Israel, Elliott E; Salam, Muhammad T MT; Galanter, Joshua J; Avila, Pedro C PC; Avila, Lydiana L; Rodriquez-Santana, Jose R JR; Chapela, Rocio R; Rodriguez-Cintron, William W; Diette, Gregory B GB; Adkinson, N Franklin NF; Abel, Rebekah A RA; Ross, Kevin D KD; Shi, Min M; Faruque, Mezbah U MU; Dunston, Georgia M GM; Watson, Harold R HR; Mantese, Vito J VJ; Ezurum, Serpil C SC; Liang, Liming L; Ruczinski, Ingo I; Ford, Jean G JG; Huntsman, Scott S; Chung, Kian Fan KF; Vora, Hita H; Li, Xia X; Calhoun, William J WJ; Castro, Mario M; Sienra-Monge, Juan J JJ; del Rio-Navarro, Blanca B; Deichmann, Klaus A KA; Heinzmann, Andrea A; Wenzel, Sally E SE; Busse, William W WW; Gern, James E JE; Lemanske, Robert F RF; Beaty, Terri H TH; Bleecker, Eugene R ER; Raby, Benjamin A BA; Meyers, Deborah A DA; London, Stephanie J SJ; , ; Gilliland, Frank D FD; , ; Burchard, Esteban G EG; , ; Martinez, Fernando D FD; , ; Weiss, Scott T ST; , ; Williams, L Keoki LK; , ; Barnes, Kathleen C KC; , ; Ober, Carole C; Nicolae, Dan L DL
Publication Date: 2011-07-31

Variant appearance in text: rs2952155
PubMed Link: 21804549
Variant Present in the following documents:
  • NIHMS304749-supplement-1.pdf
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Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer.

British Journal Of Cancer
Quaye, L L; Song, H H; Ramus, S J SJ; Gentry-Maharaj, A A; Høgdall, E E; DiCioccio, R A RA; McGuire, V V; Wu, A H AH; Van Den Berg, D J DJ; Pike, M C MC; Wozniak, E E; Doherty, J A JA; Rossing, M A MA; Ness, R B RB; Moysich, K B KB; Høgdall, C C; Blaakaer, J J; , ; Easton, D F DF; Ponder, B A J BA; Jacobs, I J IJ; Menon, U U; Whittemore, A S AS; Krüger-Kjaer, S S; Pearce, C L CL; Pharoah, P D P PD; Gayther, S A SA
Publication Date: 2009-03-24

Variant appearance in text: rs2952155
PubMed Link: 19240718
Variant Present in the following documents:
  • Main text
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Comprehensive analysis of the ATM, CHEK2 and ERBB2 genes in relation to breast tumour characteristics and survival: a population-based case-control and follow-up study.

Breast Cancer Research : Bcr
Einarsdóttir, Kristjana K; Rosenberg, Lena U LU; Humphreys, Keith K; Bonnard, Carine C; Palmgren, Juni J; Li, Yuqing Y; Li, Yi Y; Chia, Kee S KS; Liu, Edison T ET; Hall, Per P; Liu, Jianjun J; Wedrén, Sara S
Publication Date: 2006

Variant appearance in text: rs2952155
PubMed Link: 17132159
Variant Present in the following documents:
  • Main text
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HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer.

British Journal Of Cancer
Benusiglio, P R PR; Pharoah, P D PD; Smith, P L PL; Lesueur, F F; Conroy, D D; Luben, R N RN; Dew, G G; Jordan, C C; Dunning, A A; Easton, D F DF; Ponder, B A J BA
Publication Date: 2006-12-18

Variant appearance in text: rs2952155
PubMed Link: 17117180
Variant Present in the following documents:
  • Main text
  • 95-6603473a.pdf
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Common ERBB2 polymorphisms and risk of breast cancer in a white British population: a case-control study.

Breast Cancer Research : Bcr
Benusiglio, Patrick R PR; Lesueur, Fabienne F; Luccarini, Craig C; Conroy, Donald M DM; Shah, Mitul M; Easton, Douglas F DF; Day, Nick E NE; Dunning, Alison M AM; Pharoah, Paul D PD; Ponder, Bruce Aj BA
Publication Date: 2005

Variant appearance in text: rs2952155
PubMed Link: 15743501
Variant Present in the following documents:
  • Main text
  • bcr982.pdf
View BVdb publication page