AGBL4 c.952-19469C>T

Variant ID: 1-49076126-G-A

NM_032785.3(AGBL4):c.952-19469C>T

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:

Integrative mutation, haplotype and G × G interaction evidence connects ABGL4, LRP8 and PCSK9 genes to cardiometabolic risk.

Scientific Reports
Guo, Tao T; Yin, Rui-Xing RX; Yao, Li-Mei LM; Huang, Feng F; Pan, Ling L; Lin, Wei-Xiong WX; Yang, De-Zhai DZ; Pan, Shang-Ling SL
Publication Date: 2016-11-17

Variant appearance in text: AGBL4: 952-19469C>T; rs320019
PubMed Link: 27853278
Variant Present in the following documents:
  • Main text
  • srep37375.pdf
View BVdb publication page