Bibliome.ai browser hg19
Search
About
Stats
FAQ
F5 c.250+3952C>T
Variant ID: 1-169547717-G-A
NM_000130.4(
F5
):c.250+3952C>T
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: rs12755775
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Entropy based genetic association tests and gene-gene interaction tests.
Statistical Applications In Genetics And Molecular Biology
de Andrade, Mariza M; Wang, Xin X
Publication Date: 2011-08-22
Variant appearance in text: rs12755775
PubMed Link:
23089811
Variant Present in the following documents:
Main text
View BVdb publication page