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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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