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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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