NECTIN2 c.88+1876A>G

Variant ID: 19-45351746-A-G

NM_001042724.1(NECTIN2):c.88+1876A>G

This variant was identified in 8 publications

View GRCh38 version.




Publications:


APOE region molecular signatures of Alzheimer's disease across races/ethnicities.

Neurobiology Of Aging
Kulminski, Alexander M AM; Shu, Leonardo L; Loika, Yury Y; Nazarian, Alireza A; Arbeev, Konstantin K; Ukraintseva, Svetlana S; Yashin, Anatoliy A; Culminskaya, Irina I
Publication Date: 2020-03

Variant appearance in text: rs1871047
PubMed Link: 31813627
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polygenic Risk Score for Alzheimer's Disease Is Associated With Ch4 Volume in Normal Subjects.

Frontiers In Genetics
Wang, Tao T; Han, Zhifa Z; Yang, Yu Y; Tian, Rui R; Zhou, Wenyang W; Ren, Peng P; Wang, Pingping P; Zong, Jian J; Hu, Yang Y; Jiang, Qinghua Q
Publication Date: 2019

Variant appearance in text: rs1871047
PubMed Link: 31354783
Variant Present in the following documents:
  • Main text
  • fgene-10-00519.pdf
View BVdb publication page



MicroRNA-374a, -4680, and -133b suppress cell proliferation through the regulation of genes associated with human cleft palate in cultured human palate cells.

Bmc Medical Genomics
Suzuki, Akiko A; Li, Aimin A; Gajera, Mona M; Abdallah, Nada N; Zhang, Musi M; Zhao, Zhongming Z; Iwata, Junichi J
Publication Date: 2019-07-01

Variant appearance in text: rs1871047
PubMed Link: 31262291
Variant Present in the following documents:
  • 12920_2019_546_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Microglia in Alzheimer's Disease: Exploring How Genetics and Phenotype Influence Risk.

Journal Of Molecular Biology
McQuade, Amanda A; Blurton-Jones, Mathew M
Publication Date: 2019-04-19

Variant appearance in text: rs1871047
PubMed Link: 30738892
Variant Present in the following documents:
  • Main text
View BVdb publication page



Linking Alzheimer's disease and type 2 diabetes: Novel shared susceptibility genes detected by cFDR approach.

Journal Of The Neurological Sciences
Wang, Xia-Fang XF; Lin, Xu X; Li, Ding-You DY; Zhou, Rou R; Greenbaum, Jonathan J; Chen, Yuan-Cheng YC; Zeng, Chun-Ping CP; Peng, Lin-Ping LP; Wu, Ke-Hao KH; Ao, Zeng-Xin ZX; Lu, Jun-Min JM; Guo, Yan-Fang YF; Shen, Jie J; Deng, Hong-Wen HW
Publication Date: 2017-09-15

Variant appearance in text: rs1871047
PubMed Link: 28870582
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between polymorphisms in NOS3 and KCNH2 and social memory.

Frontiers In Neuroscience
Henningsson, Susanne S; Zettergren, Anna A; Hovey, Daniel D; Jonsson, Lina L; Svärd, Joakim J; Cortes, Diana S DS; Melke, Jonas J; Ebner, Natalie C NC; Laukka, Petri P; Fischer, Håkan H; Westberg, Lars L
Publication Date: 2015

Variant appearance in text: rs1871047
PubMed Link: 26539080
Variant Present in the following documents:
  • Main text
  • fnins-09-00393.pdf
View BVdb publication page



Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies.

Plos One
Pérez-Palma, Eduardo E; Bustos, Bernabé I BI; Villamán, Camilo F CF; Alarcón, Marcelo A MA; Avila, Miguel E ME; Ugarte, Giorgia D GD; Reyes, Ariel E AE; Opazo, Carlos C; De Ferrari, Giancarlo V GV; , ; ,
Publication Date: 2014

Variant appearance in text: rs1871047
PubMed Link: 24755620
Variant Present in the following documents:
  • Main text
  • pone.0095413.pdf
View BVdb publication page



Genetic evidence for the role of loci at 19q13 in cleft lip and palate.

Journal Of Medical Genetics
Warrington, A A; Vieira, A R AR; Christensen, K K; Orioli, I M IM; Castilla, E E EE; Romitti, P A PA; Murray, J C JC
Publication Date: 2006-06

Variant appearance in text: rs1871047
PubMed Link: 16740910
Variant Present in the following documents:
  • Main text
View BVdb publication page