ALK c.668-76223G>A

Variant ID: 2-30016786-C-T

NM_004304.4(ALK):c.668-76223G>A

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: rs4666275
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Predicting Triple-Negative Breast Cancer Subtype Using Multiple Single Nucleotide Polymorphisms for Breast Cancer Risk and Several Variable Selection Methods.

Geburtshilfe Und Frauenheilkunde
Häberle, Lothar L; Hein, Alexander A; Rübner, Matthias M; Schneider, Michael M; Ekici, Arif B AB; Gass, Paul P; Hartmann, Arndt A; Schulz-Wendtland, Rüdiger R; Beckmann, Matthias W MW; Lo, Wing-Yee WY; Schroth, Werner W; Brauch, Hiltrud H; Fasching, Peter A PA; Wunderle, Marius M
Publication Date: 2017-06

Variant appearance in text: rs4666275
PubMed Link: 28757654
Variant Present in the following documents:
  • Main text
View BVdb publication page