RUNDC3B c.372+1446A>G

Variant ID: 7-87331316-A-G

NM_001134405.1(RUNDC3B):c.372+1446A>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: rs6971865
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Pharmacogenetic Associations with ADME Variants and Virologic Response to an Initial HAART Regimen in HIV-Infected Women.

International Journal Of Hiv/Aids And Research
Pearce, C L CL; Stram, D D; Wiensch, A A; Frasco, M A MA; Kono, N N; Den Berg, D V DV; Anastos, K K; Cohen, M H MH; DeHovitz, J J; Golub, E T ET; Tamraz, B B; Liu, C C; Mack, W J WJ
Publication Date: 2017

Variant appearance in text: rs6971865
PubMed Link: 29577081
Variant Present in the following documents:
  • Main text
View BVdb publication page