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LIPC c.88+10326C>T
Variant ID: 15-58734645-C-T
NM_000236.2(
LIPC
):c.88+10326C>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:
A Genome-Wide Association Study of Genetic Variants of Apolipoprotein A1 Levels and Their Association with Vitamin D in Korean Cohorts.
Genes
Lee, Young Y; Yoon, Ji Won JW; Kim, Ye An YA; Choi, Hyuk Jin HJ; Yoon, Byung Woo BW; Seo, Je Hyun JH
Publication Date: 2022-08-29
Variant appearance in text: rs6494007
PubMed Link:
36140721
Variant Present in the following documents:
genes-13-01553.pdf
View BVdb publication page
Identifying potentially common genes between dyslipidemia and osteoporosis using novel analytical approaches.
Molecular Genetics And Genomics : Mgg
Lin, Xu X; Peng, Cheng C; Greenbaum, Jonathan J; Li, Zhang-Fang ZF; Wu, Ke-Hao KH; Ao, Zeng-Xin ZX; Zhang, Tong T; Shen, Jie J; Deng, Hong-Wen HW
Publication Date: 2018-06
Variant appearance in text: rs6494007
PubMed Link:
29327327
Variant Present in the following documents:
Main text
View BVdb publication page