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NEDD4L c.48+20252T>C
Variant ID: 18-55732192-T-C
NM_001144967.2(
NEDD4L
):c.48+20252T>C
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: rs4941304
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence.
Plos One
Johnson, Catherine C; Drgon, Tomas T; Walther, Donna D; Uhl, George R GR
Publication Date: 2011
Variant appearance in text: rs4941304
PubMed Link:
21818250
Variant Present in the following documents:
Main text
View BVdb publication page