KCTD10 c.388-282A>G

Variant ID: 12-109896165-T-C

NM_031954.3(KCTD10):c.388-282A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss.

American Journal Of Human Genetics
Trpchevska, Natalia N; Freidin, Maxim B MB; Broer, Linda L; Oosterloo, Berthe C BC; Yao, Shuyang S; Zhou, Yitian Y; Vona, Barbara B; Bishop, Charles C; Bizaki-Vallaskangas, Argyro A; Canlon, Barbara B; Castellana, Fabio F; Chasman, Daniel I DI; Cherny, Stacey S; Christensen, Kaare K; Concas, Maria Pina MP; Correa, Adolfo A; Elkon, Ran R; , ; Mengel-From, Jonas J; Gao, Yan Y; Giersch, Anne B S ABS; Girotto, Giorgia G; Gudjonsson, Alexander A; Gudnason, Vilmundur V; Heard-Costa, Nancy L NL; Hertzano, Ronna R; Hjelmborg, Jacob V B JVB; Hjerling-Leffler, Jens J; Hoffman, Howard J HJ; Kaprio, Jaakko J; Kettunen, Johannes J; Krebs, Kristi K; Kähler, Anna K AK; Lallemend, Francois F; Launer, Lenore J LJ; Lee, I-Min IM; Leonard, Hampton H; Li, Chuan-Ming CM; Lowenheim, Hubert H; Magnusson, Patrik K E PKE; van Meurs, Joyce J; Milani, Lili L; Morton, Cynthia C CC; Mäkitie, Antti A; Nalls, Mike A MA; Nardone, Giuseppe Giovanni GG; Nygaard, Marianne M; Palviainen, Teemu T; Pratt, Sheila S; Quaranta, Nicola N; Rämö, Joel J; Saarentaus, Elmo E; Sardone, Rodolfo R; Satizabal, Claudia L CL; Schweinfurth, John M JM; Seshadri, Sudha S; Shiroma, Eric E; Shulman, Eldad E; Simonsick, Eleanor E; Spankovich, Christopher C; Tropitzsch, Anke A; Lauschke, Volker M VM; Sullivan, Patrick F PF; Goedegebure, Andre A; Cederroth, Christopher R CR; Williams, Frances M K FMK; Nagtegaal, Andries Paul AP
Publication Date: 2022-06-02

Variant appearance in text: rs7313797
PubMed Link: 35580588
Variant Present in the following documents:
  • Main text
  • mmc3.pdf
  • main.pdf
View BVdb publication page