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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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