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.




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