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SCN1A c.4581+679G>A
Variant ID: 2-166851844-C-T
NM_001165963.1(
SCN1A
):c.4581+679G>A
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:
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: rs16851344
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
A Sparse Regression Method for Group-Wise Feature Selection with False Discovery Rate Control.
Ieee/Acm Transactions On Computational Biology And Bioinformatics
Gossmann, Alexej A; Cao, Shaolong S; Brzyski, Damian D; Zhao, Lan-Juan LJ; Deng, Hong-Wen HW; Wang, Yu-Ping YP
Publication Date: 2018
Variant appearance in text: rs16851344
PubMed Link:
29990279
Variant Present in the following documents:
Main text
View BVdb publication page