GIP c.258-73A>T

Variant ID: 17-47039254-T-A

NM_004123.2(GIP):c.258-73A>T

This variant was identified in 15 publications

View GRCh38 version.




Publications:


Comprehensive proteogenomic characterization of early duodenal cancer reveals the carcinogenesis tracks of different subtypes.

Nature Communications
Li, Lingling L; Jiang, Dongxian D; Liu, Hui H; Guo, Chunmei C; Zhao, Rui R; Zhang, Qiao Q; Xu, Chen C; Qin, Zhaoyu Z; Feng, Jinwen J; Liu, Yang Y; Wang, Haixing H; Chen, Weijie W; Zhang, Xue X; Li, Bin B; Bai, Lin L; Tian, Sha S; Tan, Subei S; Yu, Zixiang Z; Chen, Lingli L; Huang, Jie J; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C
Publication Date: 2023-03-29

Variant appearance in text: rs2291726
PubMed Link: 36991000
Variant Present in the following documents:
  • 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3
View BVdb publication page



Integrated genomic analysis identifies novel low-frequency cis-regulatory variant rs2279658 associated with VSD risk in Chinese children.

Frontiers In Cell And Developmental Biology
Jin, Lihui L; Han, Zhenyuan Z; Jiang, Zhongli Z; Lu, Jieru J; Wu, Yizhuo Y; Yan, Bingqian B; Zhang, Weibin W; Lin, Xuedong X; Jiang, Lvyan L; Zhao, Pengjun P; Sun, Kun K
Publication Date: 2022

Variant appearance in text: rs2291726
PubMed Link: 36568976
Variant Present in the following documents:
  • Main text
  • fcell-10-1062403.pdf
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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: rs2291726
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs2291726
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
View BVdb publication page



Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.

Cancer Reports (Hoboken, N.J.)
Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S
Publication Date: 2021-06

Variant appearance in text: rs2291726
PubMed Link: 33503336
Variant Present in the following documents:
  • CNR2-4-e1335-s003.xlsx, sheet 2
  • CNR2-4-e1335-s003.xlsx, sheet 1
View BVdb publication page



Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease
Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D
Publication Date: 2019-02-27

Variant appearance in text: rs2291726
PubMed Link: 30814510
Variant Present in the following documents:
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 3
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: rs2291726
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
  • Table_5.xlsx, sheet 1
View BVdb publication page



Rs46522 in the Ubiquitin-Conjugating Enzyme E2Z Gene Is Associated with the Risk of Coronary Artery Disease in Individuals of Chinese Han Population with Type 2 Diabetes.

Journal Of Diabetes Research
Lu, Difei D; Huang, Jia J; Ma, Xiaowei X; Gu, Nan N; Zhang, Junqing J; Zhang, Hong H; Guo, Xiaohui X
Publication Date: 2017

Variant appearance in text: rs2291726
PubMed Link: 28840129
Variant Present in the following documents:
  • Main text
  • JDR2017-4501794.pdf
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs2291726
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Genetic analysis for a shared biological basis between migraine and coronary artery disease.

Neurology. Genetics
Winsvold, Bendik S BS; Nelson, Christopher P CP; Malik, Rainer R; Gormley, Padhraig P; Anttila, Verneri V; Vander Heiden, Jason J; Elliott, Katherine S KS; Jacobsen, Line M LM; Palta, Priit P; Amin, Najaf N; de Vries, Boukje B; Hämäläinen, Eija E; Freilinger, Tobias T; Ikram, M Arfan MA; Kessler, Thorsten T; Koiranen, Markku M; Ligthart, Lannie L; McMahon, George G; Pedersen, Linda M LM; Willenborg, Christina C; Won, Hong-Hee HH; Olesen, Jes J; Artto, Ville V; Assimes, Themistocles L TL; Blankenberg, Stefan S; Boomsma, Dorret I DI; Cherkas, Lynn L; Davey Smith, George G; Epstein, Stephen E SE; Erdmann, Jeanette J; Ferrari, Michel D MD; Göbel, Hartmut H; Hall, Alistair S AS; Jarvelin, Marjo-Riitta MR; Kallela, Mikko M; Kaprio, Jaakko J; Kathiresan, Sekar S; Lehtimäki, Terho T; McPherson, Ruth R; März, Winfried W; Nyholt, Dale R DR; O'Donnell, Christopher J CJ; Quaye, Lydia L; Rader, Daniel J DJ; Raitakari, Olli O; Roberts, Robert R; Schunkert, Heribert H; Schürks, Markus M; Stewart, Alexandre F R AF; Terwindt, Gisela M GM; Thorsteinsdottir, Unnur U; van den Maagdenberg, Arn M J M AM; van Duijn, Cornelia C; Wessman, Maija M; Kurth, Tobias T; Kubisch, Christian C; Dichgans, Martin M; Chasman, Daniel I DI; Cotsapas, Chris C; Zwart, John-Anker JA; Samani, Nilesh J NJ; Palotie, Aarno A; ,
Publication Date: 2015-06

Variant appearance in text: rs2291726
PubMed Link: 27066539
Variant Present in the following documents:
  • Main text
  • supp_1.1.e10_Tables_e-1-e-7.pdf
  • NG2015000190.pdf
View BVdb publication page



Two novel type 2 diabetes loci revealed through integration of TCF7L2 DNA occupancy and SNP association data.

Bmj Open Diabetes Research & Care
Johnson, Matthew E ME; Zhao, Jianhua J; Schug, Jonathan J; Deliard, Sandra S; Xia, Qianghua Q; Guy, Vanessa C VC; Sainz, Jesus J; Kaestner, Klaus H KH; Wells, Andrew D AD; Grant, Struan F A SF
Publication Date: 2014

Variant appearance in text: rs2291726
PubMed Link: 25469308
Variant Present in the following documents:
  • Main text
  • bmjdrc-2014-000052.pdf
View BVdb publication page



Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

Circulation. Cardiovascular Genetics
Mehta, Nehal N NN
Publication Date: 2011-06

Variant appearance in text: rs2291726
PubMed Link: 21673312
Variant Present in the following documents:
  • Main text
View BVdb publication page



Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

Nature Genetics
Schunkert, Heribert H; König, Inke R IR; Kathiresan, Sekar S; Reilly, Muredach P MP; Assimes, Themistocles L TL; Holm, Hilma H; Preuss, Michael M; Stewart, Alexandre F R AF; Barbalic, Maja M; Gieger, Christian C; Absher, Devin D; Aherrahrou, Zouhair Z; Allayee, Hooman H; Altshuler, David D; Anand, Sonia S SS; Andersen, Karl K; Anderson, Jeffrey L JL; Ardissino, Diego D; Ball, Stephen G SG; Balmforth, Anthony J AJ; Barnes, Timothy A TA; Becker, Diane M DM; Becker, Lewis C LC; Berger, Klaus K; Bis, Joshua C JC; Boekholdt, S Matthijs SM; Boerwinkle, Eric E; Braund, Peter S PS; Brown, Morris J MJ; Burnett, Mary Susan MS; Buysschaert, Ian I; , ; Carlquist, John F JF; Chen, Li L; Cichon, Sven S; Codd, Veryan V; Davies, Robert W RW; Dedoussis, George G; Dehghan, Abbas A; Demissie, Serkalem S; Devaney, Joseph M JM; Diemert, Patrick P; Do, Ron R; Doering, Angela A; Eifert, Sandra S; Mokhtari, Nour Eddine El NE; Ellis, Stephen G SG; Elosua, Roberto R; Engert, James C JC; Epstein, Stephen E SE; de Faire, Ulf U; Fischer, Marcus M; Folsom, Aaron R AR; Freyer, Jennifer J; Gigante, Bruna B; Girelli, Domenico D; Gretarsdottir, Solveig S; Gudnason, Vilmundur V; Gulcher, Jeffrey R JR; Halperin, Eran E; Hammond, Naomi N; Hazen, Stanley L SL; Hofman, Albert A; Horne, Benjamin D BD; Illig, Thomas T; Iribarren, Carlos C; Jones, Gregory T GT; Jukema, J Wouter JW; Kaiser, Michael A MA; Kaplan, Lee M LM; Kastelein, John J P JJ; Khaw, Kay-Tee KT; Knowles, Joshua W JW; Kolovou, Genovefa G; Kong, Augustine A; Laaksonen, Reijo R; Lambrechts, Diether D; Leander, Karin K; Lettre, Guillaume G; Li, Mingyao M; Lieb, Wolfgang W; Loley, Christina C; Lotery, Andrew J AJ; Mannucci, Pier M PM; Maouche, Seraya S; Martinelli, Nicola N; McKeown, Pascal P PP; Meisinger, Christa C; Meitinger, Thomas T; Melander, Olle O; Merlini, Pier Angelica PA; Mooser, Vincent V; Morgan, Thomas T; Mühleisen, Thomas W TW; Muhlestein, Joseph B JB; Münzel, Thomas T; Musunuru, Kiran K; Nahrstaedt, Janja J; Nelson, Christopher P CP; Nöthen, Markus M MM; Olivieri, Oliviero O; Patel, Riyaz S RS; Patterson, Chris C CC; Peters, Annette A; Peyvandi, Flora F; Qu, Liming L; Quyyumi, Arshed A AA; Rader, Daniel J DJ; Rallidis, Loukianos S LS; Rice, Catherine C; Rosendaal, Frits R FR; Rubin, Diana D; Salomaa, Veikko V; Sampietro, M Lourdes ML; Sandhu, Manj S MS; Schadt, Eric E; Schäfer, Arne A; Schillert, Arne A; Schreiber, Stefan S; Schrezenmeir, Jürgen J; Schwartz, Stephen M SM; Siscovick, David S DS; Sivananthan, Mohan M; Sivapalaratnam, Suthesh S; Smith, Albert A; Smith, Tamara B TB; Snoep, Jaapjan D JD; Soranzo, Nicole N; Spertus, John A JA; Stark, Klaus K; Stirrups, Kathy K; Stoll, Monika M; Tang, W H Wilson WH; Tennstedt, Stephanie S; Thorgeirsson, Gudmundur G; Thorleifsson, Gudmar G; Tomaszewski, Maciej M; Uitterlinden, Andre G AG; van Rij, Andre M AM; Voight, Benjamin F BF; Wareham, Nick J NJ; Wells, George A GA; Wichmann, H-Erich HE; Wild, Philipp S PS; Willenborg, Christina C; Witteman, Jaqueline C M JC; Wright, Benjamin J BJ; Ye, Shu S; Zeller, Tanja T; Ziegler, Andreas A; Cambien, Francois F; Goodall, Alison H AH; Cupples, L Adrienne LA; Quertermous, Thomas T; März, Winfried W; Hengstenberg, Christian C; Blankenberg, Stefan S; Ouwehand, Willem H WH; Hall, Alistair S AS; Deloukas, Panos P; Thompson, John R JR; Stefansson, Kari K; Roberts, Robert R; Thorsteinsdottir, Unnur U; O'Donnell, Christopher J CJ; McPherson, Ruth R; Erdmann, Jeanette J; , ; Samani, Nilesh J NJ
Publication Date: 2011-03-06

Variant appearance in text: rs2291726
PubMed Link: 21378990
Variant Present in the following documents:
  • Main text
View BVdb publication page



Adaptive selection of an incretin gene in Eurasian populations.

Genome Research
Chang, Chia Lin CL; Cai, James J JJ; Lo, Chiening C; Amigo, Jorge J; Park, Jae-Il JI; Hsu, Sheau Yu Teddy SY
Publication Date: 2011-01

Variant appearance in text: rs2291726
PubMed Link: 20978139
Variant Present in the following documents:
  • Main text
View BVdb publication page



A case-control analysis of common variants in GIP with type 2 diabetes and related biochemical parameters in a South Indian population.

Bmc Medical Genetics
Sugunan, Divya D; Nair, Anup K AK; Kumar, Harish H; Gopalakrishnapillai, Anilkumar A
Publication Date: 2010-07-30

Variant appearance in text: rs2291726
PubMed Link: 20673334
Variant Present in the following documents:
  • Main text
  • 1471-2350-11-118.pdf
View BVdb publication page