CFTR c.2619+3333T>G

Variant ID: 7-117238445-T-G

NM_000492.3(CFTR):c.2619+3333T>G

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: rs213977
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



MGST2 and WNT2 are candidate genes for comitant strabismus susceptibility in Japanese patients.

Peerj
Zhang, Jingjing J; Matsuo, Toshihiko T
Publication Date: 2017

Variant appearance in text: rs213977
PubMed Link: 29062608
Variant Present in the following documents:
  • Main text
  • peerj-05-3935.pdf
View BVdb publication page