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CFTR c.2909-413A>C
Variant ID: 7-117246315-A-C
NM_000492.3(
CFTR
):c.2909-413A>C
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Frequency of allele variations in the CFTR gene in a Mexican population.
Bmc Medical Genomics
Cantú-Reyna, Consuelo C; Galindo-Ramírez, Roberto R; Vázquez-Cantú, Mercedes M; Haddad-Talancón, Lorenza L; García-Muñoz, Willebaldo W
Publication Date: 2021-11-05
Variant appearance in text: rs2299445
PubMed Link:
34740355
Variant Present in the following documents:
12920_2021_1111_MOESM1_ESM.xlsx, sheet 1
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: rs2299445
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: rs2299445
PubMed Link:
29062608
Variant Present in the following documents:
Main text
peerj-05-3935.pdf
View BVdb publication page