CFTR c.2619+3341A>C

CFTR c.2619+3341A>C

Variant ID: 7-117238453-A-C

NM_000492.3(CFTR):c.2619+3341A>C

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: rs4148714

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: rs4148714

PubMed Link: 29062608

Variant Present in the following documents:

Main text

peerj-05-3935.pdf

View BVdb publication page