TGFBR3 c.62-8892G>A

Variant ID: 1-92271920-C-T

NM_003243.4(TGFBR3):c.62-8892G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Transforming Growth Factor Beta Receptor 3 Haplotypes in Sickle Cell Disease Are Associated with Lipid Profile and Clinical Manifestations.

Mediators Of Inflammation
Santiago, Rayra P RP; Figueiredo, Camylla V B CVB; Fiuza, Luciana M LM; Yahouédéhou, Sètondji C M A SCMA; Oliveira, Rodrigo M RM; Aleluia, Milena M MM; Carvalho, Suellen P SP; Fonseca, Cleverson A CA; Nascimento, Valma M L VML; Rocha, Larissa C LC; Guarda, Caroline C CC; Gonçalves, Marilda S MS
Publication Date: 2020

Variant appearance in text: rs284157
PubMed Link: 33149723
Variant Present in the following documents:
  • Main text
  • MI2020-3185015.pdf
View BVdb publication page



Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

Genomics Insights
Driss, A A; Asare, K O KO; Hibbert, J M JM; Gee, B E BE; Adamkiewicz, T V TV; Stiles, J K JK
Publication Date: 2009-07-30

Variant appearance in text: rs284157
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
View BVdb publication page



Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.

Blood
Baldwin, Clinton C; Nolan, Vikki G VG; Wyszynski, Diego F DF; Ma, Qian-Li QL; Sebastiani, Paola P; Embury, Stephen H SH; Bisbee, Alice A; Farrell, John J; Farrer, Lindsay L; Steinberg, Martin H MH
Publication Date: 2005-07-01

Variant appearance in text: rs284157
PubMed Link: 15784727
Variant Present in the following documents:
  • Main text
View BVdb publication page