ST8SIA6 c.377+13370G>A

Variant ID: 10-17388143-C-T

NM_001004470.1(ST8SIA6):c.377+13370G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Rare genetic variants and treatment response: sample size and analysis issues.

Statistics In Medicine
Witte, John S JS
Publication Date: 2012-11-10

Variant appearance in text: rs359312
PubMed Link: 22736504
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

American Journal Of Epidemiology
Panagiotou, Orestis A OA; Evangelou, Evangelos E; Ioannidis, John P A JP
Publication Date: 2010-10-15

Variant appearance in text: rs359312
PubMed Link: 20876667
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association studies in pharmacogenomics: successes and lessons.

Pharmacogenetics And Genomics
Motsinger-Reif, Alison A AA; Jorgenson, Eric E; Relling, Mary V MV; Kroetz, Deanna L DL; Weinshilboum, Richard R; Cox, Nancy J NJ; Roden, Dan M DM
Publication Date: 2013-08

Variant appearance in text: rs359312
PubMed Link: 20639796
Variant Present in the following documents:
  • Main text
View BVdb publication page