Bibliome.ai browser hg19
Search
About
Stats
FAQ
ZPR1 c.*4492T>C
Variant ID: 11-116645149-A-G
NM_003904.3(
ZPR1
):c.*4492T>C
This variant was identified in 4 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
A genome-wide search for gene-by-obesity interaction loci of dyslipidemia in Koreans shows diverse genetic risk alleles.
Journal Of Lipid Research
Kang, Moonil M; Sung, Joohon J
Publication Date: 2019-12
Variant appearance in text: rs2041967
PubMed Link:
31662442
Variant Present in the following documents:
Main text
View BVdb publication page
Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, India.
Human Genomics
Pranavchand, Rayabarapu R; Kumar, Arramraju Sreenivas AS; Reddy, Battini Mohan BM
Publication Date: 2017-03-04
Variant appearance in text: rs2041967
PubMed Link:
28257648
Variant Present in the following documents:
Main text
40246_2017_Article_99.pdf
View BVdb publication page
Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.
Plos One
Pranav Chand, Rayabarapu R; Kumar, Arramraju Sreenivas AS; Anuj, Kapadia K; Vishnupriya, Satti S; Mohan Reddy, Battini B
Publication Date: 2016
Variant appearance in text: rs2041967
PubMed Link:
27257688
Variant Present in the following documents:
Main text
pone.0153720.pdf
View BVdb publication page
Haplotype analysis of the apolipoprotein gene cluster on human chromosome 11.
Genomics
Olivier, Michael M; Wang, Xujing X; Cole, Regina R; Gau, Brian B; Kim, Jessica J; Rubin, Edward M EM; Pennacchio, Len A LA
Publication Date: 2004-05
Variant appearance in text: rs2041967
PubMed Link:
15081120
Variant Present in the following documents:
Main text
View BVdb publication page