LDLR c.68-2917T>C

Variant ID: 19-11207982-T-C

NM_000527.4(LDLR):c.68-2917T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change.

Npj Genomic Medicine
Oni-Orisan, Akinyemi A; Haldar, Tanushree T; Ranatunga, Dilrini K DK; Medina, Marisa W MW; Schaefer, Catherine C; Krauss, Ronald M RM; Iribarren, Carlos C; Risch, Neil N; Hoffmann, Thomas J TJ
Publication Date: 2020

Variant appearance in text: rs67337506
PubMed Link: 31969989
Variant Present in the following documents:
  • Main text
  • 41525_2019_Article_109.pdf
View BVdb publication page



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: rs67337506
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page