TNFRSF11A c.76-4953A>C

Variant ID: 18-60010448-A-C

NM_003839.3(TNFRSF11A):c.76-4953A>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Chia, Ruth R; Saez-Atienzar, Sara S; Murphy, Natalie N; ChiĆ², Adriano A; Blauwendraat, Cornelis C; , ; Roda, Ricardo H RH; Tienari, Pentti J PJ; Kaminski, Henry J HJ; Ricciardi, Roberta R; Guida, Melania M; De Rosa, Anna A; Petrucci, Loredana L; Evoli, Amelia A; Provenzano, Carlo C; Drachman, Daniel B DB; Traynor, Bryan J BJ
Publication Date: 2022-02-01

Variant appearance in text: rs4369774
PubMed Link: 35074870
Variant Present in the following documents:
  • Main text
View BVdb publication page



RANKL and OPG Polymorphisms Are Associated with Aromatase Inhibitor-Related Musculoskeletal Adverse Events in Chinese Han Breast Cancer Patients.

Plos One
Wang, Jingxuan J; Lu, Kangping K; Song, Ying Y; Zhao, Shu S; Ma, Wenjie W; Xuan, Qijia Q; Tang, Dabei D; Zhao, Hong H; Liu, Lei L; Zhang, Qingyuan Q
Publication Date: 2015

Variant appearance in text: rs4369774
PubMed Link: 26218592
Variant Present in the following documents:
  • Main text
  • pone.0133964.pdf
View BVdb publication page