Bibliome.ai browser hg19
Search
About
Stats
FAQ
SLCO1B1 c.85-13121G>A
Variant ID: 12-21312463-G-A
NM_006446.4(
SLCO1B1
):c.85-13121G>A
This variant was identified in 2 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: rs3899743
PubMed Link:
34852805
Variant Present in the following documents:
Main text
12911_2021_Article_1701.pdf
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: rs3899743
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page