ABCC4 c.1824+1934T>C

Variant ID: 13-95820852-A-G

NM_005845.3(ABCC4):c.1824+1934T>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


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: rs9561797
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Analysis of ABCG2 and other urate transporters in uric acid homeostasis in chronic kidney disease: potential role of remote sensing and signaling.

Clinical Kidney Journal
Bhatnagar, Vibha V; Richard, Erin L EL; Wu, Wei W; Nievergelt, Caroline M CM; Lipkowitz, Michael S MS; Jeff, Janina J; Maihofer, Adam X AX; Nigam, Sanjay K SK
Publication Date: 2016-06

Variant appearance in text: rs9561797
PubMed Link: 27274832
Variant Present in the following documents:
  • Main text
  • sfw010.pdf
View BVdb publication page



Genetic variations and patient-reported quality of life among patients with lung cancer.

Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology
Sloan, Jeff A JA; de Andrade, Mariza M; Decker, Paul P; Wampfler, Jason J; Oswold, Curtis C; Clark, Matthew M; Yang, Ping P
Publication Date: 2012-05-10

Variant appearance in text: rs9561797
PubMed Link: 22454423
Variant Present in the following documents:
  • Main text
View BVdb publication page