LRP2 c.79+7454C>T

Variant ID: 2-170211377-G-A

NM_004525.2(LRP2):c.79+7454C>T

This variant was identified in 5 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: rs2389557
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



The Association of Vitamin D and Its Pathway Genes' Polymorphisms with Hypertensive Disorders of Pregnancy: A Prospective Cohort Study.

Nutrients
Si, Shuting S; Mo, Minjia M; Cheng, Haoyue H; Peng, Zhicheng Z; Alifu, Xialidan X; Zhou, Haibo H; Chi, Peihan P; Zhuang, Yan Y; Yu, Yunxian Y
Publication Date: 2022-06-06

Variant appearance in text: rs2389557
PubMed Link: 35684156
Variant Present in the following documents:
  • Main text
  • nutrients-14-02355.pdf
View BVdb publication page



Association of Selenoprotein and Selenium Pathway Genotypes with Risk of Colorectal Cancer and Interaction with Selenium Status.

Nutrients
Fedirko, Veronika V; Jenab, Mazda M; Méplan, Catherine C; Jones, Jeb S JS; Zhu, Wanzhe W; Schomburg, Lutz L; Siddiq, Afshan A; Hybsier, Sandra S; Overvad, Kim K; Tjønneland, Anne A; Omichessan, Hanane H; Perduca, Vittorio V; Boutron-Ruault, Marie-Christine MC; Kühn, Tilman T; Katzke, Verena V; Aleksandrova, Krasimira K; Trichopoulou, Antonia A; Karakatsani, Anna A; Kotanidou, Anastasia A; Tumino, Rosario R; Panico, Salvatore S; Masala, Giovanna G; Agnoli, Claudia C; Naccarati, Alessio A; Bueno-de-Mesquita, Bas B; Vermeulen, Roel C H RCH; Weiderpass, Elisabete E; Skeie, Guri G; Nøst, Therese Haugdahl TH; Lujan-Barroso, Leila L; Quirós, J Ramón JR; Huerta, José María JM; Rodríguez-Barranco, Miguel M; Barricarte, Aurelio A; Gylling, Björn B; Harlid, Sophia S; Bradbury, Kathryn E KE; Wareham, Nick N; Khaw, Kay-Tee KT; Gunter, Marc M; Murphy, Neil N; Freisling, Heinz H; Tsilidis, Kostas K; Aune, Dagfinn D; Riboli, Elio E; Hesketh, John E JE; Hughes, David J DJ
Publication Date: 2019-04-25

Variant appearance in text: rs2389557
PubMed Link: 31027226
Variant Present in the following documents:
  • Main text
  • nutrients-11-00935.pdf
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Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.

Bmc Medical Genetics
Pangilinan, Faith F; Molloy, Anne M AM; Mills, James L JL; Troendle, James F JF; Parle-McDermott, Anne A; Signore, Caroline C; O'Leary, Valerie B VB; Chines, Peter P; Seay, Jessica M JM; Geiler-Samerotte, Kerry K; Mitchell, Adam A; VanderMeer, Julia E JE; Krebs, Kristine M KM; Sanchez, Angelica A; Cornman-Homonoff, Joshua J; Stone, Nicole N; Conley, Mary M; Kirke, Peadar N PN; Shane, Barry B; Scott, John M JM; Brody, Lawrence C LC
Publication Date: 2012-08-02

Variant appearance in text: rs2389557
PubMed Link: 22856873
Variant Present in the following documents:
  • Main text
  • 1471-2350-13-62.pdf
View BVdb publication page



Association between low density lipoprotein receptor-related protein 2 gene polymorphisms and bone mineral density variation in Chinese population.

Plos One
Wang, Chun C; Hu, Yi-Ming YM; He, Jin-Wei JW; Gu, Jie-Mei JM; Zhang, Hao H; Hu, Wei-Wei WW; Yue, Hua H; Gao, Gao G; Xiao, Wen-Jin WJ; Yu, Jin-Bo JB; Ke, Yao-Hua YH; Hu, Yun-Qiu YQ; Li, Miao M; Liu, Yu-Juan YJ; Fu, Wen-Zhen WZ; Ren, Ying Y; Zhang, Zhen-Lin ZL
Publication Date: 2011

Variant appearance in text: rs2389557
PubMed Link: 22174918
Variant Present in the following documents:
  • Main text
  • pone.0028874.pdf
View BVdb publication page