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SPHKAP c.4449-4252G>A
Variant ID: 2-228864662-C-T
NM_001142644.1(
SPHKAP
):c.4449-4252G>A
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Epigenome wide association study of SNP-CpG interactions on changes in triglyceride levels after pharmaceutical intervention: a GAW20 analysis.
Bmc Proceedings
Veenstra, Jenna J; Kalsbeek, Anya A; Koster, Karissa K; Ryder, Nathan N; Bos, Abbey A; Huisman, Jordan J; VanderBerg, Lucas L; VanderWoude, Jason J; Tintle, Nathan L NL
Publication Date: 2018
Variant appearance in text: rs11680053
PubMed Link:
30275900
Variant Present in the following documents:
Main text
View BVdb publication page
Bayesian Network Construction and Genotype-Phenotype Inference Using GWAS Statistics.
Ieee/Acm Transactions On Computational Biology And Bioinformatics
Zhang, Lu L; Pan, Qiuping Q; Wang, Yue Y; Wu, Xintao X; Shi, Xinghua X
Publication Date: 2019
Variant appearance in text: rs11680053
PubMed Link:
29990020
Variant Present in the following documents:
Main text
View BVdb publication page
Local Ancestry and Clinical Cardiovascular Events Among African Americans From the Atherosclerosis Risk in Communities Study.
Journal Of The American Heart Association
Shendre, Aditi A; Irvin, Marguerite R MR; Wiener, Howard H; Zhi, Degui D; Limdi, Nita A NA; Overton, Edgar T ET; Shrestha, Sadeep S
Publication Date: 2017-04-10
Variant appearance in text: rs11680053
PubMed Link:
28396569
Variant Present in the following documents:
Main text
View BVdb publication page