Bibliome.ai browser hg19
Search
About
Stats
FAQ
LIPG c.*1506T>C
Variant ID: 18-47118398-T-C
NM_006033.2(
LIPG
):c.*1506T>C
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:
APOE and KLF14 genetic variants are sex-specific for low high-density lipoprotein cholesterol identified by a genome-wide association study.
Genetics And Molecular Biology
Lee, Ying-Hui YH; Chang, Ya-Sian YS; Hsieh, Chih-Chang CC; Wang, Rong-Tsorng RT; Chang, Jan-Gowth JG; Chen, Chung-Jen CJ; Chang, Shun-Jen SJ
Publication Date: 2022
Variant appearance in text: rs9958734
PubMed Link:
35238325
Variant Present in the following documents:
Main text
1415-4757-GMB-45-1-e20210280.pdf
View BVdb publication page
Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.
Bmc Cardiovascular Disorders
Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M
Publication Date: 2020-02-11
Variant appearance in text: rs9958734
PubMed Link:
32046637
Variant Present in the following documents:
12872_2020_1369_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page