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SLCO1B3 c.334T>C ;(p.S112P)
Variant ID: 12-21011480-T-C
NM_019844.3(
SLCO1B3
):c.334T>C;(p.S112P)
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:
Identification of two novel genes SLC15A2 and SLCO1B3 associated with maintenance dose variability of warfarin in a Chinese population.
Scientific Reports
Cai, Liang-Liang LL; Huang, Wen-Qing WQ; Su, Zhi-Ying ZY; Ye, Hui-Ming HM; Wang, Lian-Sheng LS; Wu, Yuan Y; Zhang, Zhong-Ying ZY; Zhang, Wei W; Tzeng, Chi-Meng CM
Publication Date: 2017-12-12
Variant appearance in text: N/A
PubMed Link:
29234073
Variant Present in the following documents:
View BVdb publication page
Pharmacogenetic Foundations of Therapeutic Efficacy and Adverse Events of Statins.
International Journal Of Molecular Sciences
Arrigoni, Elena E; Del Re, Marzia M; Fidilio, Leonardo L; Fogli, Stefano S; Danesi, Romano R; Di Paolo, Antonello A
Publication Date: 2017-01-06
Variant appearance in text: SLCO1B3: 334T>C; rs4149117
PubMed Link:
28067828
Variant Present in the following documents:
Main text
ijms-18-00104.pdf
View BVdb publication page