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SLCO1B1 c.680G>C ;(p.G227A)
Variant ID: 12-21331907-G-C
NM_006446.4(
SLCO1B1
):c.680G>C;(p.G227A)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genetic variants associated with gastrointestinal symptoms in Fabry disease.
Oncotarget
Di Martino, Maria Teresa MT; Scionti, Francesca F; Sestito, Simona S; Nicoletti, Angela A; Arbitrio, Mariamena M; Hiram Guzzi, Pietro P; Talarico, Valentina V; Altomare, Federica F; Sanseviero, Maria Teresa MT; Agapito, Giuseppe G; Pisani, Antonio A; Riccio, Eleonora E; Borrelli, Osvaldo O; Concolino, Daniela D; Pensabene, Licia L
Publication Date: 2016-12-27
Variant appearance in text: SLCO1B1: 680G>C
PubMed Link:
27825144
Variant Present in the following documents:
Main text
View BVdb publication page