TGFB3 c.926+623G>C

Variant ID: 14-76429036-C-G

NM_003239.2(TGFB3):c.926+623G>C

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Genetic Risk Assessment of Nonsyndromic Cleft Lip with or without Cleft Palate by Linking Genetic Networks and Deep Learning Models.

International Journal Of Molecular Sciences
Kang, Geon G; Baek, Seung-Hak SH; Kim, Young Ho YH; Kim, Dong-Hyun DH; Park, Ji Wan JW
Publication Date: 2023-02-25

Variant appearance in text: rs2284791
PubMed Link: 36901988
Variant Present in the following documents:
  • ijms-24-04557.pdf
View BVdb publication page



The Genetic Architecture of the Etiology of Lower Extremity Peripheral Artery Disease: Current Knowledge and Future Challenges in the Era of Genomic Medicine.

International Journal Of Molecular Sciences
Butnariu, Lăcrămioara Ionela LI; Gorduza, Eusebiu Vlad EV; Florea, Laura L; Țarcă, Elena E; Moisă, Ștefana Maria ȘM; Tradafir, Laura Mihaela LM; Cojocaru, Elena E; Luca, Alina-Costina AC; Stătescu, Laura L; Bădescu, Minerva Codruța MC
Publication Date: 2022-09-09

Variant appearance in text: rs2284791
PubMed Link: 36142394
Variant Present in the following documents:
  • ijms-23-10481.pdf
View BVdb publication page



Transforming growth factor-β signaling pathway-associated genes SMAD2 and TGFBR2 are implicated in metabolic syndrome in a Taiwanese population.

Scientific Reports
Lin, Eugene E; Kuo, Po-Hsiu PH; Liu, Yu-Li YL; Yang, Albert C AC; Tsai, Shih-Jen SJ
Publication Date: 2017-10-19

Variant appearance in text: rs2284791
PubMed Link: 29051557
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_14025.pdf
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs2284791
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Complexity in the genetic architecture of leukoaraiosis in hypertensive sibships from the GENOA Study.

Bmc Medical Genomics
Smith, Jennifer A JA; Turner, Stephen T ST; Sun, Yan V YV; Fornage, Myriam M; Kelly, Reagan J RJ; Mosley, Thomas H TH; Jack, Clifford R CR; Kullo, Iftikhar J IJ; Kardia, Sharon L R SL
Publication Date: 2009-04-07

Variant appearance in text: rs2284791
PubMed Link: 19351393
Variant Present in the following documents:
  • Main text
View BVdb publication page



Investigating the complex genetic architecture of ankle-brachial index, a measure of peripheral arterial disease, in non-Hispanic whites.

Bmc Medical Genomics
Kardia, Sharon Lr SL; Greene, M Todd MT; Boerwinkle, Eric E; Turner, Stephen T ST; Kullo, Iftikhar J IJ
Publication Date: 2008-05-15

Variant appearance in text: rs2284791
PubMed Link: 18482449
Variant Present in the following documents:
  • Main text
  • 1755-8794-1-16.pdf
View BVdb publication page