LDLRAP1 c.274G>A ;(p.V92M)

Variant ID: 1-25881393-G-A

NM_015627.2(LDLRAP1):c.274G>A;(p.V92M)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Effects of familial hypercholesterolemia-associated genes on the phenotype of premature myocardial infarction.

Lipids In Health And Disease
Lee, Chongyou C; Cui, Yuxia Y; Song, Junxian J; Li, Sufang S; Zhang, Feng F; Wu, Manyan M; Li, Long L; Hu, Dan D; Chen, Hong H
Publication Date: 2019-04-11

Variant appearance in text: LDLRAP1: 274G>A; Val92Met
PubMed Link: 30971288
Variant Present in the following documents:
  • Main text
  • 12944_2019_Article_1042.pdf
View BVdb publication page



Prevalence of familial hypercholesterolemia in patients with premature myocardial infarction.

Clinical Cardiology
Cui, Yuxia Y; Li, Sufang S; Zhang, Feng F; Song, Junxian J; Lee, Chongyou C; Wu, Manyan M; Chen, Hong H
Publication Date: 2019-03

Variant appearance in text: LDLRAP1: 274G>A; Val92Met
PubMed Link: 30637778
Variant Present in the following documents:
  • Main text
  • CLC-42-385.pdf
View BVdb publication page