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APOC3 c.-14+119C>T
Variant ID: 11-116700775-C-T
NM_000040.3(
APOC3
):c.-14+119C>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:
An APOC3 3'UTR variant associated with plasma triglycerides levels and coronary heart disease by creating a functional miR-4271 binding site.
Scientific Reports
Hu, Sen-Lin SL; Cui, Guang-Lin GL; Huang, Jin J; Jiang, Jian-Gang JG; Wang, Dao-Wen DW
Publication Date: 2016-09-14
Variant appearance in text: rs12721090
PubMed Link:
27624799
Variant Present in the following documents:
Main text
srep32700.pdf
View BVdb publication page