LDLR c.2389+116G>T

Variant ID: 19-11238877-G-T

NM_000527.4(LDLR):c.2389+116G>T

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: rs2304182
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
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Association analysis of 33 lipoprotein candidate genes in multi-generational families of African ancestry.

Journal Of Lipid Research
Miljkovic, I I; Yerges-Armstrong, L M LM; Kuller, L H LH; Kuipers, A L AL; Wang, X X; Kammerer, C M CM; Nestlerode, C S CS; Bunker, C H CH; Patrick, A L AL; Wheeler, V W VW; Evans, R W RW; Zmuda, J M JM
Publication Date: 2010-07

Variant appearance in text: rs2304182
PubMed Link: 20308432
Variant Present in the following documents:
  • Main text
View BVdb publication page