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CETP c.234-48C>T
Variant ID: 16-57003250-C-T
NM_000078.2(
CETP
):c.234-48C>T
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:
Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.
Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017
Variant appearance in text: rs13306230
PubMed Link:
28690861
Variant Present in the following documents:
hgv201727-s1.xls, sheet 1
View BVdb publication page
Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits.
Plos Genetics
Zhang, Futao F; Xie, Dan D; Liang, Meimei M; Xiong, Momiao M
Publication Date: 2016-04
Variant appearance in text: rs13306230
PubMed Link:
27104857
Variant Present in the following documents:
Main text
pgen.1005965.pdf
View BVdb publication page