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F5 c.374-3262C>A
Variant ID: 1-169533266-G-T
NM_000130.4(
F5
):c.374-3262C>A
This variant was identified in 4 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: rs6678795
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Targeted next-generation resequencing of f5 gene identifies novel multiple variants pattern in severe hereditary factor v deficiency.
Case Reports In Genetics
Janicki, Piotr K PK; Vaida, Sonia S; Al-Mondhiry, Hamid A B HA
Publication Date: 2013
Variant appearance in text: rs6678795
PubMed Link:
23662219
Variant Present in the following documents:
Main text
CRIM.GENETICS2013-941684.pdf
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: rs6678795
PubMed Link:
23089811
Variant Present in the following documents:
Main text
View BVdb publication page
Simultaneous analysis of multiple data types in pharmacogenomic studies using weighted sparse canonical correlation analysis.
Omics : A Journal Of Integrative Biology
Chalise, Prabhakar P; Batzler, Anthony A; Abo, Ryan R; Wang, Liewei L; Fridley, Brooke L BL
Publication Date: 2012
Variant appearance in text: rs6678795
PubMed Link:
22734853
Variant Present in the following documents:
Main text
View BVdb publication page