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.




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