RUNDC3B c.239-3612T>G

Variant ID: 7-87326125-T-G

NM_001134405.1(RUNDC3B):c.239-3612T>G

This variant was identified in 2 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: rs12670317
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Pathway-based analysis using genome-wide association data from a Korean non-small cell lung cancer study.

Plos One
Lee, Donghoon D; Lee, Geon Kook GK; Yoon, Kyong-Ah KA; Lee, Jin Soo JS
Publication Date: 2013

Variant appearance in text: rs12670317
PubMed Link: 23762359
Variant Present in the following documents:
  • Main text
  • pone.0065396.pdf
View BVdb publication page