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LPCAT3 c.151+11504A>C
Variant ID: 12-7114074-T-G
NM_005768.5(
LPCAT3
):c.151+11504A>C
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Candidate pathway-based genome-wide association studies identify novel associations of genomic variants in the complement system associated with coronary artery disease.
Circulation. Cardiovascular Genetics
Xu, Chengqi C; Yang, Qin Q; Xiong, Hongbo H; Wang, Longfei L; Cai, Jianping J; Wang, Fan F; Li, Sisi S; Chen, Jing J; Wang, Chuchu C; Wang, Dan D; Xiong, Xin X; Wang, Pengyun P; Zhao, Yuanyuan Y; Wang, Xiaojing X; Huang, Yufeng Y; Chen, Shanshan S; Yin, Dan D; Li, Xiuchun X; Liu, Ying Y; Liu, Jinqiu J; Wang, Jingjing J; Li, Hui H; Ke, Tie T; Ren, Xiang X; Wu, Yanxia Y; Wu, Gang G; Wan, Jing J; Zhang, Rongfeng R; Wu, Tangchun T; Wang, Junhan J; Xia, Yunlong Y; Yang, Yanzong Y; Cheng, Xiang X; Liao, Yuhua Y; Chen, Qiuyun Q; Zhou, Yanhong Y; He, Qing Q; Tu, Xin X; Wang, Qing K QK
Publication Date: 2014-12
Variant appearance in text: rs34962575
PubMed Link:
25249547
Variant Present in the following documents:
Main text
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