Bibliome.ai browser hg19
Search
About
Stats
FAQ
LDLR c.68-4038G>A
Variant ID: 19-11206861-G-A
NM_000527.4(
LDLR
):c.68-4038G>A
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:
Role of non-coding variants in cardiovascular disease.
Journal Of Cellular And Molecular Medicine
Heshmatzad, Katayoun K; Naderi, Niloofar N; Maleki, Majid M; Abbasi, Shiva S; Ghasemi, Serwa S; Ashrafi, Nooshin N; Fazelifar, Amir Farjam AF; Mahdavi, Mohammad M; Kalayinia, Samira S
Publication Date: 2023-05-15
Variant appearance in text: rs17242388
PubMed Link:
37183561
Variant Present in the following documents:
Main text
View BVdb publication page
Rare non-coding variants are associated with plasma lipid traits in a founder population.
Scientific Reports
Igartua, Catherine C; Mozaffari, Sahar V SV; Nicolae, Dan L DL; Ober, Carole C
Publication Date: 2017-11-27
Variant appearance in text: rs17242388
PubMed Link:
29180722
Variant Present in the following documents:
Main text
41598_2017_Article_16550.pdf
41598_2017_16550_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page