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SLCO1B1 c.1683-396A>G
Variant ID: 12-21374838-A-G
NM_006446.4(
SLCO1B1
):c.1683-396A>G
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:
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: rs987839
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS).
Neurobiology Of Aging
Shi, Hui H; Belbin, Olivia O; Medway, Christopher C; Brown, Kristelle K; Kalsheker, Noor N; Carrasquillo, Minerva M; Proitsi, Petroula P; Powell, John J; Lovestone, Simon S; Goate, Alison A; Younkin, Steven S; Passmore, Peter P; , ; Morgan, Kevin K; ,
Publication Date: 2012-08
Variant appearance in text: rs987839
PubMed Link:
22445811
Variant Present in the following documents:
Main text
View BVdb publication page