TF c.326-381G>A

Variant ID: 3-133472958-G-A

NM_001063.3(TF):c.326-381G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.

British Journal Of Haematology
Constantine, Clare C CC; Anderson, Greg J GJ; Vulpe, Chris D CD; McLaren, Christine E CE; Bahlo, Melanie M; Yeap, Heng Lin HL; Gertig, Dorota M DM; Osborne, Nicholas J NJ; Bertalli, Nadine A NA; Beckman, Kenneth B KB; Chen, Victoria V; Matak, Pavel P; McKie, Andrew T AT; Delatycki, Martin B MB; Olynyk, John K JK; English, Dallas R DR; Southey, Melissa C MC; Giles, Graham G GG; Hopper, John L JL; Allen, Katrina J KJ; Gurrin, Lyle C LC
Publication Date: 2009-10

Variant appearance in text: rs8177215
PubMed Link: 19673882
Variant Present in the following documents:
  • Main text
View BVdb publication page