GFRA1 c.771-4576A>G

Variant ID: 10-117860851-T-C

NM_005264.4(GFRA1):c.771-4576A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Data on a genome-wide association study of type 2 diabetes in a Maya population.

Data In Brief
Totomoch-Serra, Armando A; Domínguez-Cruz, Miriam Givisay MG; Muñoz, María de Lourdes ML; García-Escalante, María Guadalupe MG; Burgueño, Juan J; Díaz-Badillo, Álvaro Á; Valadez-González, Nina N; Escalante, Doris Pinto DP
Publication Date: 2020-02

Variant appearance in text: rs17094083
PubMed Link: 31872004
Variant Present in the following documents:
  • Main text
View BVdb publication page



A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.

Plos One
Östensson, Malin M; Montén, Caroline C; Bacelis, Jonas J; Gudjonsdottir, Audur H AH; Adamovic, Svetlana S; Ek, Johan J; Ascher, Henry H; Pollak, Elisabet E; Arnell, Henrik H; Browaldh, Lars L; Agardh, Daniel D; Wahlström, Jan J; Nilsson, Staffan S; Torinsson-Naluai, Åsa Å
Publication Date: 2013

Variant appearance in text: rs17094083
PubMed Link: 23936387
Variant Present in the following documents:
  • Main text
  • pone.0070174.pdf
View BVdb publication page