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SLCO1B1 c.481+165A>T
Variant ID: 12-21329996-A-T
NM_006446.4(
SLCO1B1
):c.481+165A>T
This variant was identified in 4 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Ensemble learning for the early prediction of neonatal jaundice with genetic features.
Bmc Medical Informatics And Decision Making
Deng, Haowen H; Zhou, Youyou Y; Wang, Lin L; Zhang, Cheng C
Publication Date: 2021-12-01
Variant appearance in text: rs4149044
PubMed Link:
34852805
Variant Present in the following documents:
Main text
12911_2021_Article_1701.pdf
View BVdb publication page
Genetic Diversity in Drug Transporters: Impact in African Populations.
Clinical And Translational Science
Rajman, Iris I; Knapp, Laura L; Hanna, Imad I
Publication Date: 2020-09
Variant appearance in text: rs4149044
PubMed Link:
32100958
Variant Present in the following documents:
Main text
CTS-13-848.pdf
View BVdb publication page
Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.
Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018
Variant appearance in text: SLCO1B1: 481+165A>T; rs4149044
PubMed Link:
30319441
Variant Present in the following documents:
Table_7.xlsx, sheet 1
Table_6.xlsx, sheet 1
View BVdb publication page
Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.
The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04
Variant appearance in text: rs4149044
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page