LRRC34 c.1192-519G>T

Variant ID: 3-169512145-C-A

NM_001172779.1(LRRC34):c.1192-519G>T

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Variability in newborn telomere length is explained by inheritance and intrauterine environment.

Bmc Medicine
Chen, Li L; Ling, Karen Tan Mei KTM; Gong, Min M; Chong, Mary F F MFF; Tan, Kok Hian KH; Chong, Yap Seng YS; Meaney, Michael J MJ; Gluckman, Peter D PD; Eriksson, Johan G JG; Karnani, Neerja N
Publication Date: 2022-01-25

Variant appearance in text: rs7621631
PubMed Link: 35073935
Variant Present in the following documents:
  • Main text
  • 12916_2021_Article_2217.pdf
View BVdb publication page



Variability in newborn telomere length is explained by inheritance and intrauterine environment.

Bmc Medicine
Chen, Li L; Tan, Karen Mei Ling KML; Gong, Min M; Chong, Mary F F MFF; Tan, Kok Hian KH; Chong, Yap Seng YS; Meaney, Michael J MJ; Gluckman, Peter D PD; Eriksson, Johan G JG; Karnani, Neerja N
Publication Date: 2022-01-25

Variant appearance in text: rs7621631
PubMed Link: 35073935
Variant Present in the following documents:
  • Main text
  • 12916_2021_Article_2217.pdf
View BVdb publication page



Tracking the Genetic Susceptibility Background of B-Cell Non-Hodgkin's Lymphomas from Genome-Wide Association Studies.

International Journal Of Molecular Sciences
Hernández-Verdin, Isaias I; Labreche, Karim K; Benazra, Marion M; Mokhtari, Karima K; Hoang-Xuan, Khê K; Alentorn, Agusti A
Publication Date: 2020-12-24

Variant appearance in text: rs7621631
PubMed Link: 33374413
Variant Present in the following documents:
  • Main text
  • ijms-22-00122.pdf
View BVdb publication page



Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length.

American Journal Of Human Genetics
Li, Chen C; Stoma, Svetlana S; Lotta, Luca A LA; Warner, Sophie S; Albrecht, Eva E; Allione, Alessandra A; Arp, Pascal P PP; Broer, Linda L; Buxton, Jessica L JL; Da Silva Couto Alves, Alexessander A; Deelen, Joris J; Fedko, Iryna O IO; Gordon, Scott D SD; Jiang, Tao T; Karlsson, Robert R; Kerrison, Nicola N; Loe, Taylor K TK; Mangino, Massimo M; Milaneschi, Yuri Y; Miraglio, Benjamin B; Pervjakova, Natalia N; Russo, Alessia A; Surakka, Ida I; van der Spek, Ashley A; Verhoeven, Josine E JE; Amin, Najaf N; Beekman, Marian M; Blakemore, Alexandra I AI; Canzian, Federico F; Hamby, Stephen E SE; Hottenga, Jouke-Jan JJ; Jones, Peter D PD; Jousilahti, Pekka P; Mägi, Reedik R; Medland, Sarah E SE; Montgomery, Grant W GW; Nyholt, Dale R DR; Perola, Markus M; Pietiläinen, Kirsi H KH; Salomaa, Veikko V; Sillanpää, Elina E; Suchiman, H Eka HE; van Heemst, Diana D; Willemsen, Gonneke G; Agudo, Antonio A; Boeing, Heiner H; Boomsma, Dorret I DI; Chirlaque, Maria-Dolores MD; Fagherazzi, Guy G; Ferrari, Pietro P; Franks, Paul P; Gieger, Christian C; Eriksson, Johan Gunnar JG; Gunter, Marc M; Hägg, Sara S; Hovatta, Iiris I; Imaz, Liher L; Kaprio, Jaakko J; Kaaks, Rudolf R; Key, Timothy T; Krogh, Vittorio V; Martin, Nicholas G NG; Melander, Olle O; Metspalu, Andres A; Moreno, Concha C; Onland-Moret, N Charlotte NC; Nilsson, Peter P; Ong, Ken K KK; Overvad, Kim K; Palli, Domenico D; Panico, Salvatore S; Pedersen, Nancy L NL; Penninx, Brenda W J H BWJH; Quirós, J Ramón JR; Jarvelin, Marjo Riitta MR; Rodríguez-Barranco, Miguel M; Scott, Robert A RA; Severi, Gianluca G; Slagboom, P Eline PE; Spector, Tim D TD; Tjonneland, Anne A; Trichopoulou, Antonia A; Tumino, Rosario R; Uitterlinden, André G AG; van der Schouw, Yvonne T YT; van Duijn, Cornelia M CM; Weiderpass, Elisabete E; Denchi, Eros Lazzerini EL; Matullo, Giuseppe G; Butterworth, Adam S AS; Danesh, John J; Samani, Nilesh J NJ; Wareham, Nicholas J NJ; Nelson, Christopher P CP; Langenberg, Claudia C; Codd, Veryan V
Publication Date: 2020-03-05

Variant appearance in text: rs7621631
PubMed Link: 32109421
Variant Present in the following documents:
  • mmc2.xlsx, sheet 9
View BVdb publication page



Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.

Genetic Epidemiology
Din, Lennox L; Sheikh, Mohammad M; Kosaraju, Nikitha N; Smedby, Karin Ekstrom KE; Bernatsky, Sasha S; Berndt, Sonja I SI; Skibola, Christine F CF; Nieters, Alexandra A; Wang, Sophia S; McKay, James D JD; Cocco, Pierluigi P; Maynadié, Marc M; Foretová, Lenka L; Staines, Anthony A; Mack, Thomas M TM; de Sanjosé, Silvia S; Vyse, Timothy J TJ; Padyukov, Leonid L; Monnereau, Alain A; Arslan, Alan A AA; Moore, Amy A; Brooks-Wilson, Angela R AR; Novak, Anne J AJ; Glimelius, Bengt B; Birmann, Brenda M BM; Link, Brian K BK; Stewart, Carolyn C; Vajdic, Claire M CM; Haioun, Corinne C; Magnani, Corrado C; Conti, David V DV; Cox, David G DG; Casabonne, Delphine D; Albanes, Demetrius D; Kane, Eleanor E; Roman, Eve E; Muzi, Giacomo G; Salles, Gilles G; Giles, Graham G GG; Adami, Hans-Olov HO; Ghesquières, Hervé H; De Vivo, Immaculata I; Clavel, Jacqueline J; Cerhan, James R JR; Spinelli, John J JJ; Hofmann, Jonathan J; Vijai, Joseph J; Curtin, Karen K; Costenbader, Karen H KH; Onel, Kenan K; Offit, Kenneth K; Teras, Lauren R LR; Morton, Lindsay L; Conde, Lucia L; Miligi, Lucia L; Melbye, Mads M; Ennas, Maria Grazia MG; Liebow, Mark M; Purdue, Mark P MP; Glenn, Martha M; Southey, Melissa C MC; Din, Morris M; Rothman, Nathaniel N; Camp, Nicola J NJ; Wong Doo, Nicole N; Becker, Nikolaus N; Pradhan, Nisha N; Bracci, Paige M PM; Boffetta, Paolo P; Vineis, Paolo P; Brennan, Paul P; Kraft, Peter P; Lan, Qing Q; Severson, Richard K RK; Vermeulen, Roel C H RCH; Milne, Roger L RL; Kaaks, Rudolph R; Travis, Ruth C RC; Weinstein, Stephanie J SJ; Chanock, Stephen J SJ; Ansell, Stephen M SM; Slager, Susan L SL; Zheng, Tongzhang T; Zhang, Yawei Y; Benavente, Yolanda Y; Taub, Zachary Z; Madireddy, Lohith L; Gourraud, Pierre-Antoine PA; Oksenberg, Jorge R JR; Cozen, Wendy W; Hjalgrim, Henrik H; Khankhanian, Pouya P
Publication Date: 2019-10

Variant appearance in text: rs7621631
PubMed Link: 31407831
Variant Present in the following documents:
  • Main text
View BVdb publication page



A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.

Bmc Genomics
Fernandez-Rozadilla, Ceres C; Cazier, Jean-Baptiste JB; Tomlinson, Ian P IP; Carvajal-Carmona, Luis G LG; Palles, Claire C; Lamas, María J MJ; Baiget, Montserrat M; López-Fernández, Luis A LA; Brea-Fernández, Alejandro A; Abulí, Anna A; Bujanda, Luis L; Clofent, Juan J; Gonzalez, Dolors D; Xicola, Rosa R; Andreu, Montserrat M; Bessa, Xavier X; Jover, Rodrigo R; Llor, Xavier X; , ; Moreno, Víctor V; Castells, Antoni A; Carracedo, Ángel Á; Castellvi-Bel, Sergi S; Ruiz-Ponte, Clara C
Publication Date: 2013-01-26

Variant appearance in text: rs7621631
PubMed Link: 23350875
Variant Present in the following documents:
  • Main text
  • 1471-2164-14-55.pdf
View BVdb publication page