Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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