AGO2 c.22+10255A>G

Variant ID: 8-141635329-T-C

NM_012154.3(AGO2):c.22+10255A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure.

Nature Communications
Levin, Michael G MG; Tsao, Noah L NL; Singhal, Pankhuri P; Liu, Chang C; Vy, Ha My T HMT; Paranjpe, Ishan I; Backman, Joshua D JD; Bellomo, Tiffany R TR; Bone, William P WP; Biddinger, Kiran J KJ; Hui, Qin Q; Dikilitas, Ozan O; Satterfield, Benjamin A BA; Yang, Yifan Y; Morley, Michael P MP; Bradford, Yuki Y; Burke, Megan M; Reza, Nosheen N; Charest, Brian B; , ; Judy, Renae L RL; Puckelwartz, Megan J MJ; Hakonarson, Hakon H; Khan, Atlas A; Kottyan, Leah C LC; Kullo, Iftikhar I; Luo, Yuan Y; McNally, Elizabeth M EM; Rasmussen-Torvik, Laura J LJ; Day, Sharlene M SM; Do, Ron R; Phillips, Lawrence S LS; Ellinor, Patrick T PT; Nadkarni, Girish N GN; Ritchie, Marylyn D MD; Arany, Zoltan Z; Cappola, Thomas P TP; Margulies, Kenneth B KB; Aragam, Krishna G KG; Haggerty, Christopher M CM; Joseph, Jacob J; Sun, Yan V YV; Voight, Benjamin F BF; Damrauer, Scott M SM
Publication Date: 2022-11-14

Variant appearance in text: rs1962104
PubMed Link: 36376295
Variant Present in the following documents:
  • 41467_2022_Article_34216.pdf
View BVdb publication page



A combined genome-wide association and molecular study of age-related hearing loss in H. sapiens.

Bmc Medicine
Liu, Wei W; Johansson, Åsa Å; Rask-Andersen, Helge H; Rask-Andersen, Mathias M
Publication Date: 2021-12-01

Variant appearance in text: rs1962104
PubMed Link: 34847940
Variant Present in the following documents:
  • Main text
  • 12916_2021_Article_2169.pdf
View BVdb publication page



A combined genome-wide association and molecular study of age-related hearing loss in H. sapiens.

Bmc Medicine
Liu, Wei W; Johansson, Åsa Å; Rask-Andersen, Helge H; Rask-Andersen, Mathias M
Publication Date: 2021-12-01

Variant appearance in text: rs1962104
PubMed Link: 34847940
Variant Present in the following documents:
  • Main text
  • 12916_2021_Article_2169.pdf
View BVdb publication page



Item-level analyses reveal genetic heterogeneity in neuroticism.

Nature Communications
Nagel, Mats M; Watanabe, Kyoko K; Stringer, Sven S; Posthuma, Danielle D; van der Sluis, Sophie S
Publication Date: 2018-03-02

Variant appearance in text: rs1962104
PubMed Link: 29500382
Variant Present in the following documents:
  • 41467_2018_3242_MOESM2_ESM.pdf
View BVdb publication page