HFE c.617-48C>G

Variant ID: 6-26092865-C-G

NM_000410.3(HFE):c.617-48C>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Comprehensive analysis of HFE gene in hereditary hemochromatosis and in diseases associated with acquired iron overload.

World Journal Of Hepatology
de Campos, Wagner Narciso WN; Massaro, Juliana Doblas JD; Cançado, Eduardo Luiz Rachid ELR; Wiezel, Cláudia Emília Vieira CEV; Simões, Aguinaldo Luiz AL; Teixeira, Andreza Correa AC; de Souza, Fernanda Fernandes FF; Mendes-Junior, Celso Teixeira CT; Martinelli, Ana de Lourdes Candolo ALC; Donadi, Eduardo Antônio EA
Publication Date: 2019-02-27

Variant appearance in text: rs807209
PubMed Link: 30820268
Variant Present in the following documents:
  • Main text
  • WJH-11-186.pdf
View BVdb publication page



Haplotype analysis of the HFE gene among populations of Northern Eurasia, in patients with metabolic disorders or stomach cancer, and in long-lived people.

Bmc Genetics
Mikhailova, S V SV; Babenko, V N VN; Ivanoshchuk, D E DE; Gubina, M A MA; Maksimov, V N VN; Solovjova, I G IG; Voevoda, M I MI
Publication Date: 2016-06-17

Variant appearance in text: rs807209
PubMed Link: 27317329
Variant Present in the following documents:
  • Main text
  • 12863_2016_Article_396.pdf
View BVdb publication page