ALK c.953-41006A>C

Variant ID: 2-29795988-T-G

NM_004304.4(ALK):c.953-41006A>C

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: rs13014477
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Pharmacogenomics of selective serotonin reuptake inhibitor treatment for major depressive disorder: genome-wide associations and functional genomics.

The Pharmacogenomics Journal
Ji, Y Y; Biernacka, J M JM; Hebbring, S S; Chai, Y Y; Jenkins, G D GD; Batzler, A A; Snyder, K A KA; Drews, M S MS; Desta, Z Z; Flockhart, D D; Mushiroda, T T; Kubo, M M; Nakamura, Y Y; Kamatani, N N; Schaid, D D; Weinshilboum, R M RM; Mrazek, D A DA
Publication Date: 2013-10

Variant appearance in text: rs13014477
PubMed Link: 22907730
Variant Present in the following documents:
  • Main text
View BVdb publication page