RUNDC3B c.123-1378G>A

Variant ID: 7-87278760-G-A

NM_001134405.1(RUNDC3B):c.123-1378G>A

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Pharmacogenetics of tenofovir and emtricitabine penetration into cerebrospinal fluid.

Southern African Journal Of Hiv Medicine
Decloedt, Eric H EH; Sinxadi, Phumla Z PZ; Wiesner, Lubbe L; Joska, John A JA; Haas, David W DW; Maartens, Gary G
Publication Date: 2021

Variant appearance in text: rs10267099
PubMed Link: 34007475
Variant Present in the following documents:
  • Main text
View BVdb publication page



Ethnogeographic and inter-individual variability of human ABC transporters.

Human Genetics
Xiao, Qingyang Q; Zhou, Yitian Y; Lauschke, Volker M VM
Publication Date: 2020-05

Variant appearance in text: rs10267099
PubMed Link: 32206879
Variant Present in the following documents:
  • Main text
  • 439_2020_Article_2150.pdf
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs10267099
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Polymorphisms and pharmacogenomics for the toxicity of methotrexate monotherapy in patients with rheumatoid arthritis: A systematic review and meta-analysis.

Medicine
Qiu, Qi Q; Huang, Jing J; Lin, Yang Y; Shu, Xiaoming X; Fan, Huizheng H; Tu, Zhihua Z; Zhou, Youwen Y; Xiao, Cheng C
Publication Date: 2017-03

Variant appearance in text: rs10267099
PubMed Link: 28296761
Variant Present in the following documents:
  • medi-96-e6337.pdf
View BVdb publication page



Atenolol induced HDL-C change in the pharmacogenomic evaluation of antihypertensive responses (PEAR) study.

Plos One
McDonough, Caitrin W CW; Gillis, Nancy K NK; Alsultan, Abdullah A; Chang, Shin-Wen SW; Kawaguchi-Suzuki, Marina M; Lang, Jason E JE; Shahin, Mohamed Hossam A MH; Buford, Thomas W TW; El Rouby, Nihal M NM; Sá, Ana C C AC; Langaee, Taimour Y TY; Gums, John G JG; Chapman, Arlene B AB; Cooper-DeHoff, Rhonda M RM; Turner, Stephen T ST; Gong, Yan Y; Johnson, Julie A JA
Publication Date: 2013

Variant appearance in text: rs10267099
PubMed Link: 24116192
Variant Present in the following documents:
  • Main text
  • pone.0076984.pdf
View BVdb publication page



Single nucleotide polymorphisms and risk of recurrence of renal-cell carcinoma: a cohort study.

The Lancet. Oncology
Schutz, Fabio A B FA; Pomerantz, Mark M MM; Gray, Kathryn P KP; Atkins, Michael B MB; Rosenberg, Jonathan E JE; Hirsch, Michelle S MS; McDermott, David F DF; Lampron, Megan E ME; Lee, Gwo-Shu Mary GS; Signoretti, Sabina S; Kantoff, Philip W PW; Freedman, Matthew L ML; Choueiri, Toni K TK
Publication Date: 2013-01

Variant appearance in text: rs10267099
PubMed Link: 23219378
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of pharmacogenetic traits in two distinct South African populations.

Human Genomics
Ikediobi, Ogechi O; Aouizerat, Bradley B; Xiao, Yuanyuan Y; Gandhi, Monica M; Gebhardt, Stefan S; Warnich, Louise L
Publication Date: 2011-05

Variant appearance in text: rs10267099
PubMed Link: 21712189
Variant Present in the following documents:
  • Main text
View BVdb publication page