NECTIN2 c.479-2756T>G

Variant ID: 19-45372354-T-G

NM_001042724.1(NECTIN2):c.479-2756T>G

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Genetic and regulatory architecture of Alzheimer's disease in the APOE region.

Alzheimer'S & Dementia (Amsterdam, Netherlands)
Kulminski, Alexander M AM; Shu, Leonardo L; Loika, Yury Y; He, Liang L; Nazarian, Alireza A; Arbeev, Konstantin K; Ukraintseva, Svetlana S; Yashin, Anatoliy A; Culminskaya, Irina I
Publication Date: 2020

Variant appearance in text: rs8104483
PubMed Link: 32211503
Variant Present in the following documents:
  • Main text
  • DAD2-12-e12008.pdf
  • DAD2-12-e12008-s007.xlsx, sheet 1
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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: rs8104483
PubMed Link: 32160291
Variant Present in the following documents:
  • Main text
  • ddaa033.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: rs8104483
PubMed Link: 31346172
Variant Present in the following documents:
  • 41467_2019_10945_MOESM1_ESM.pdf
View BVdb publication page



Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging.

Molecular Psychiatry
Yan, Qi Q; Nho, Kwangsik K; Del-Aguila, Jorge L JL; Wang, Xingbin X; Risacher, Shannon L SL; Fan, Kang-Hsien KH; Snitz, Beth E BE; Aizenstein, Howard J HJ; Mathis, Chester A CA; Lopez, Oscar L OL; Demirci, F Yesim FY; Feingold, Eleanor E; Klunk, William E WE; Saykin, Andrew J AJ; , ; Cruchaga, Carlos C; Kamboh, M Ilyas MI
Publication Date: 2021-01

Variant appearance in text: rs8104483
PubMed Link: 30361487
Variant Present in the following documents:
  • Main text
  • 41380_2018_Article_246.pdf
View BVdb publication page



Apolipoprotein E region molecular signatures of Alzheimer's disease.

Aging Cell
Kulminski, Alexander M AM; Huang, Jian J; Wang, Jiayi J; He, Liang L; Loika, Yury Y; Culminskaya, Irina I
Publication Date: 2018-08

Variant appearance in text: rs8104483
PubMed Link: 29797398
Variant Present in the following documents:
  • Main text
  • ACEL-17-na.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: rs8104483
PubMed Link: 28438747
Variant Present in the following documents:
  • benm033277.ww1.pdf
View BVdb publication page



A systematic heritability analysis of the human whole blood transcriptome.

Human Genetics
Huan, Tianxiao T; Liu, Chunyu C; Joehanes, Roby R; Zhang, Xiaoling X; Chen, Brian H BH; Johnson, Andrew D AD; Yao, Chen C; Courchesne, Paul P; O'Donnell, Christopher J CJ; Munson, Peter J PJ; Levy, Daniel D
Publication Date: 2015-03

Variant appearance in text: rs8104483
PubMed Link: 25585846
Variant Present in the following documents:
  • Main text
View BVdb publication page



Performance of random forest when SNPs are in linkage disequilibrium.

Bmc Bioinformatics
Meng, Yan A YA; Yu, Yi Y; Cupples, L Adrienne LA; Farrer, Lindsay A LA; Lunetta, Kathryn L KL
Publication Date: 2009-03-05

Variant appearance in text: rs8104483
PubMed Link: 19265542
Variant Present in the following documents:
  • Main text
  • 1471-2105-10-78.pdf
View BVdb publication page