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.




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