APOB c.2067+1G>A

Variant ID: 2-21250699-C-T

NM_000384.2(APOB):c.2067+1G>A

This variant was identified in 1 publication

View GRCh38 version.



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

Publications:

Clinical utility of genomic analysis in adults with idiopathic liver disease.

Journal Of Hepatology
Hakim, Aaron A; Zhang, Xuchen X; DeLisle, Angela A; Oral, Elif A EA; Dykas, Daniel D; Drzewiecki, Kaela K; Assis, David N DN; Silveira, Marina M; Batisti, Jennifer J; Jain, Dhanpat D; Bale, Allen A; Mistry, Pramod K PK; Vilarinho, Silvia S
Publication Date: 2019-06

Variant appearance in text: APOB: 2067+1G>A
PubMed Link: 31000363
Variant Present in the following documents:
  • Main text
View BVdb publication page