NECTIN2 c.479-1545G>A

Variant ID: 19-45373565-G-A

NM_001042724.1(NECTIN2):c.479-1545G>A

This variant was identified in 12 publications

View GRCh38 version.




Publications:


TOMM40 genetic variants associated with healthy aging and longevity: a systematic review.

Bmc Geriatrics
Chen, Sunny S; Sarasua, Sara M SM; Davis, Nicole J NJ; DeLuca, Jane M JM; Boccuto, Luigi L; Thielke, Stephen M SM; Yu, Chang-En CE
Publication Date: 2022-08-13

Variant appearance in text: rs395908
PubMed Link: 35964003
Variant Present in the following documents:
  • Main text
  • 12877_2022_Article_3337.pdf
View BVdb publication page



A polygenic biomarker to identify patients with severe hypercholesterolemia of polygenic origin.

Molecular Genetics & Genomic Medicine
Leal, Luis G LG; Hoggart, Clive C; Jarvelin, Marjo-Riitta MR; Herzig, Karl-Heinz KH; Sternberg, Michael J E MJE; David, Alessia A
Publication Date: 2020-06

Variant appearance in text: rs395908
PubMed Link: 32307928
Variant Present in the following documents:
  • Main text
View BVdb publication page



DNA methylation QTL analysis identifies new regulators of human longevity.

Human Molecular Genetics
Szymczak, Silke S; Dose, Janina J; Torres, Guillermo G GG; Heinsen, Femke-Anouska FA; Venkatesh, Geetha G; Datlinger, Paul P; Nygaard, Marianne M; Mengel-From, Jonas J; Flachsbart, Friederike F; Klapper, Wolfram W; Christensen, Kaare K; Lieb, Wolfgang W; Schreiber, Stefan S; Häsler, Robert R; Bock, Christoph C; Franke, Andre A; Nebel, Almut A
Publication Date: 2020-05-08

Variant appearance in text: rs395908
PubMed Link: 32160291
Variant Present in the following documents:
  • Main text
  • ddaa033.pdf
View BVdb publication page



A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context.

Nature Communications
Gallois, Apolline A; Mefford, Joel J; Ko, Arthur A; Vaysse, Amaury A; Julienne, Hanna H; Ala-Korpela, Mika M; Laakso, Markku M; Zaitlen, Noah N; Pajukanta, Päivi P; Aschard, Hugues H
Publication Date: 2019-10-21

Variant appearance in text: rs395908
PubMed Link: 31636271
Variant Present in the following documents:
  • Main text
  • 41467_2019_Article_12703.pdf
View BVdb publication page



Non-coding variability at the APOE locus contributes to the Alzheimer's risk.

Nature Communications
Zhou, Xiaopu X; Chen, Yu Y; Mok, Kin Y KY; Kwok, Timothy C Y TCY; Mok, Vincent C T VCT; Guo, Qihao Q; Ip, Fanny C FC; Chen, Yuewen Y; Mullapudi, Nandita N; , ; Giusti-Rodríguez, Paola P; Sullivan, Patrick F PF; Hardy, John J; Fu, Amy K Y AKY; Li, Yun Y; Ip, Nancy Y NY
Publication Date: 2019-07-25

Variant appearance in text: rs395908
PubMed Link: 31346172
Variant Present in the following documents:
  • 41467_2019_10945_MOESM1_ESM.pdf
View BVdb publication page



Genetics of Human Longevity From Incomplete Data: New Findings From the Long Life Family Study.

The Journals Of Gerontology. Series A, Biological Sciences And Medical Sciences
Yashin, Anatoliy I AI; Arbeev, Konstantin G KG; Wu, Deqing D; Arbeeva, Liubov S LS; Bagley, Olivia O; Stallard, Eric E; Kulminski, Alexander M AM; Akushevich, Igor I; Fang, Fang F; Wojczynski, Mary K MK; Christensen, Kaare K; Newman, Anne B AB; Boudreau, Robert M RM; Province, Michael A MA; Thielke, Stephen S; Perls, Thomas T TT; An, Ping P; Elo, Irma I; Ukraintseva, Svetlana V SV
Publication Date: 2018-10-08

Variant appearance in text: rs395908
PubMed Link: 30299504
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of genetic risk factors in the Chinese population implicates a role of immune system in Alzheimer's disease pathogenesis.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Zhou, Xiaopu X; Chen, Yu Y; Mok, Kin Y KY; Zhao, Qianhua Q; Chen, Keliang K; Chen, Yuewen Y; Hardy, John J; Li, Yun Y; Fu, Amy K Y AKY; Guo, Qihao Q; Ip, Nancy Y NY; ,
Publication Date: 2018-02-20

Variant appearance in text: rs395908
PubMed Link: 29432188
Variant Present in the following documents:
  • pnas.1715554115.sapp.pdf
View BVdb publication page



Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.

Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24

Variant appearance in text: rs395908
PubMed Link: 28438747
Variant Present in the following documents:
  • benm033277.ww1.pdf
View BVdb publication page



Genetic variants in PVRL2-TOMM40-APOE region are associated with human longevity in a Han Chinese population.

Plos One
Lu, Fang F; Guan, Huaijin H; Gong, Bo B; Liu, Xiaoqi X; Zhu, Rongrong R; Wang, Yong Y; Qian, Jingjing J; Zhou, Tianqiu T; Lan, Xiaoyan X; Wang, Pu P; Lin, Ying Y; Ma, Shi S; Lin, He H; Zhu, Xiong X; Chen, Rong R; Zhu, Xianjun X; Shi, Yi Y; Yang, Zhenglin Z
Publication Date: 2014

Variant appearance in text: rs395908
PubMed Link: 24924924
Variant Present in the following documents:
  • Main text
  • pone.0099580.pdf
View BVdb publication page



Genome-wide association study of genetic determinants of LDL-c response to atorvastatin therapy: importance of Lp(a).

Journal Of Lipid Research
Deshmukh, Harshal A HA; Colhoun, Helen M HM; Johnson, Toby T; McKeigue, Paul M PM; Betteridge, D John DJ; Durrington, Paul N PN; Fuller, John H JH; Livingstone, Shona S; Charlton-Menys, Valentine V; Neil, Andrew A; Poulter, Neil N; Sever, Peter P; Shields, Denis C DC; Stanton, Alice V AV; Chatterjee, Aurobindo A; Hyde, Craig C; Calle, Roberto A RA; DeMicco, David A DA; Trompet, Stella S; Postmus, Iris I; Ford, Ian I; Jukema, J Wouter JW; Caulfield, Mark M; Hitman, Graham A GA
Publication Date: 2012-05

Variant appearance in text: rs395908
PubMed Link: 22368281
Variant Present in the following documents:
  • Main text
  • 1000.pdf
View BVdb publication page



Biological, clinical and population relevance of 95 loci for blood lipids.

Nature
Teslovich, Tanya M TM; Musunuru, Kiran K; Smith, Albert V AV; Edmondson, Andrew C AC; Stylianou, Ioannis M IM; Koseki, Masahiro M; Pirruccello, James P JP; Ripatti, Samuli S; Chasman, Daniel I DI; Willer, Cristen J CJ; Johansen, Christopher T CT; Fouchier, Sigrid W SW; Isaacs, Aaron A; Peloso, Gina M GM; Barbalic, Maja M; Ricketts, Sally L SL; Bis, Joshua C JC; Aulchenko, Yurii S YS; Thorleifsson, Gudmar G; Feitosa, Mary F MF; Chambers, John J; Orho-Melander, Marju M; Melander, Olle O; Johnson, Toby T; Li, Xiaohui X; Guo, Xiuqing X; Li, Mingyao M; Shin Cho, Yoon Y; Jin Go, Min M; Jin Kim, Young Y; Lee, Jong-Young JY; Park, Taesung T; Kim, Kyunga K; Sim, Xueling X; Twee-Hee Ong, Rick R; Croteau-Chonka, Damien C DC; Lange, Leslie A LA; Smith, Joshua D JD; Song, Kijoung K; Hua Zhao, Jing J; Yuan, Xin X; Luan, Jian'an J; Lamina, Claudia C; Ziegler, Andreas A; Zhang, Weihua W; Zee, Robert Y L RY; Wright, Alan F AF; Witteman, Jacqueline C M JC; Wilson, James F JF; Willemsen, Gonneke G; Wichmann, H-Erich HE; Whitfield, John B JB; Waterworth, Dawn M DM; Wareham, Nicholas J NJ; Waeber, Gérard G; Vollenweider, Peter P; Voight, Benjamin F BF; Vitart, Veronique V; Uitterlinden, Andre G AG; Uda, Manuela M; Tuomilehto, Jaakko J; Thompson, John R JR; Tanaka, Toshiko T; Surakka, Ida I; Stringham, Heather M HM; Spector, Tim D TD; Soranzo, Nicole N; Smit, Johannes H JH; Sinisalo, Juha J; Silander, Kaisa K; Sijbrands, Eric J G EJ; Scuteri, Angelo A; Scott, James J; Schlessinger, David D; Sanna, Serena S; Salomaa, Veikko V; Saharinen, Juha J; Sabatti, Chiara C; Ruokonen, Aimo A; Rudan, Igor I; Rose, Lynda M LM; Roberts, Robert R; Rieder, Mark M; Psaty, Bruce M BM; Pramstaller, Peter P PP; Pichler, Irene I; Perola, Markus M; Penninx, Brenda W J H BW; Pedersen, Nancy L NL; Pattaro, Cristian C; Parker, Alex N AN; Pare, Guillaume G; Oostra, Ben A BA; O'Donnell, Christopher J CJ; Nieminen, Markku S MS; Nickerson, Deborah A DA; Montgomery, Grant W GW; Meitinger, Thomas T; McPherson, Ruth R; McCarthy, Mark I MI; McArdle, Wendy W; Masson, David D; Martin, Nicholas G NG; Marroni, Fabio F; Mangino, Massimo M; Magnusson, Patrik K E PK; Lucas, Gavin G; Luben, Robert R; Loos, Ruth J F RJ; Lokki, Marja-Liisa ML; Lettre, Guillaume G; Langenberg, Claudia C; Launer, Lenore J LJ; Lakatta, Edward G EG; Laaksonen, Reijo R; Kyvik, Kirsten O KO; Kronenberg, Florian F; König, Inke R IR; Khaw, Kay-Tee KT; Kaprio, Jaakko J; Kaplan, Lee M LM; Johansson, Asa A; Jarvelin, Marjo-Riitta MR; Janssens, A Cecile J W AC; Ingelsson, Erik E; Igl, Wilmar W; Kees Hovingh, G G; Hottenga, Jouke-Jan JJ; Hofman, Albert A; Hicks, Andrew A AA; Hengstenberg, Christian C; Heid, Iris M IM; Hayward, Caroline C; Havulinna, Aki S AS; Hastie, Nicholas D ND; Harris, Tamara B TB; Haritunians, Talin T; Hall, Alistair S AS; Gyllensten, Ulf U; Guiducci, Candace C; Groop, Leif C LC; Gonzalez, Elena E; Gieger, Christian C; Freimer, Nelson B NB; Ferrucci, Luigi L; Erdmann, Jeanette J; Elliott, Paul P; Ejebe, Kenechi G KG; Döring, Angela A; Dominiczak, Anna F AF; Demissie, Serkalem S; Deloukas, Panagiotis P; de Geus, Eco J C EJ; de Faire, Ulf U; Crawford, Gabriel G; Collins, Francis S FS; Chen, Yii-der I YD; Caulfield, Mark J MJ; Campbell, Harry H; Burtt, Noel P NP; Bonnycastle, Lori L LL; Boomsma, Dorret I DI; Boekholdt, S Matthijs SM; Bergman, Richard N RN; Barroso, Inês I; Bandinelli, Stefania S; Ballantyne, Christie M CM; Assimes, Themistocles L TL; Quertermous, Thomas T; Altshuler, David D; Seielstad, Mark M; Wong, Tien Y TY; Tai, E-Shyong ES; Feranil, Alan B AB; Kuzawa, Christopher W CW; Adair, Linda S LS; Taylor, Herman A HA; Borecki, Ingrid B IB; Gabriel, Stacey B SB; Wilson, James G JG; Holm, Hilma H; Thorsteinsdottir, Unnur U; Gudnason, Vilmundur V; Krauss, Ronald M RM; Mohlke, Karen L KL; Ordovas, Jose M JM; Munroe, Patricia B PB; Kooner, Jaspal S JS; Tall, Alan R AR; Hegele, Robert A RA; Kastelein, John J P JJ; Schadt, Eric E EE; Rotter, Jerome I JI; Boerwinkle, Eric E; Strachan, David P DP; Mooser, Vincent V; Stefansson, Kari K; Reilly, Muredach P MP; Samani, Nilesh J NJ; Schunkert, Heribert H; Cupples, L Adrienne LA; Sandhu, Manjinder S MS; Ridker, Paul M PM; Rader, Daniel J DJ; van Duijn, Cornelia M CM; Peltonen, Leena L; Abecasis, Gonçalo R GR; Boehnke, Michael M; Kathiresan, Sekar S
Publication Date: 2010-08-05

Variant appearance in text: rs395908
PubMed Link: 20686565
Variant Present in the following documents:
  • NIHMS213289-supplement-1.pdf
View BVdb publication page



Sequence variants in host cell factor C1 are associated with Ménière's disease.

Otology & Neurotology : Official Publication Of The American Otological Society, American Neurotology Society [And] European Academy Of Otology And Neurotology
Vrabec, Jeffrey T JT; Liu, Liqian L; Li, Bingshan B; Leal, Suzanne M SM
Publication Date: 2008-06

Variant appearance in text: rs395908
PubMed Link: 18520591
Variant Present in the following documents:
  • Main text
View BVdb publication page