CFTR c.1392+395G>C

Variant ID: 7-117189272-G-C

NM_000492.3(CFTR):c.1392+395G>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The CFTR gene variants in Japanese children with idiopathic pancreatitis.

Human Genome Variation
Iso, Manami M; Suzuki, Mitsuyoshi M; Yanagi, Kumiko K; Minowa, Kei K; Sakurai, Yumiko Y; Nakano, Satoshi S; Satou, Kazuhito K; Shimizu, Toshiaki T; Kaname, Tadashi T
Publication Date: 2019

Variant appearance in text: rs1820871
PubMed Link: 30992994
Variant Present in the following documents:
  • Main text
  • 41439_2019_Article_49.pdf
View BVdb publication page



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: rs1820871
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page