ALK c.952+41373C>T

Variant ID: 2-29876343-G-A

NM_004304.4(ALK):c.952+41373C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Replication analysis of variants associated with multiple sclerosis risk.

Scientific Reports
Dashti, Mohammad M; Ateyah, Khadijah K; Alroughani, Raed R; Al-Temaimi, Rabeah R
Publication Date: 2020-04-30

Variant appearance in text: rs7577363
PubMed Link: 32355262
Variant Present in the following documents:
  • 41598_2020_64432_MOESM1_ESM.pdf
View BVdb publication page



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: rs7577363
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page