ADGRV1 c.18153-17266T>C

Variant ID: 5-90350998-T-C

NM_032119.3(ADGRV1):c.18153-17266T>C

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: rs16869392
PubMed Link: 31872004
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.

Circulation. Cardiovascular Genetics
Guo, Tingwei T; Repetto, Gabriela M GM; McDonald McGinn, Donna M DM; Chung, Jonathan H JH; Nomaru, Hiroko H; Campbell, Christopher L CL; Blonska, Anna A; Bassett, Anne S AS; Chow, Eva W C EWC; Mlynarski, Elisabeth E EE; Swillen, Ann A; Vermeesch, Joris J; Devriendt, Koen K; Gothelf, Doron D; Carmel, Miri M; Michaelovsky, Elena E; Schneider, Maude M; Eliez, Stephan S; Antonarakis, Stylianos E SE; Coleman, Karlene K; Tomita-Mitchell, Aoy A; Mitchell, Michael E ME; Digilio, M Cristina MC; Dallapiccola, Bruno B; Marino, Bruno B; Philip, Nicole N; Busa, Tiffany T; Kushan-Wells, Leila L; Bearden, Carrie E CE; Piotrowicz, Małgorzata M; Hawuła, Wanda W; Roberts, Amy E AE; Tassone, Flora F; Simon, Tony J TJ; van Duin, Esther D A EDA; van Amelsvoort, Thérèse A TA; Kates, Wendy R WR; Zackai, Elaine E; Johnston, H Richard HR; Cutler, David J DJ; Agopian, A J AJ; Goldmuntz, Elizabeth E; Mitchell, Laura E LE; Wang, Tao T; Emanuel, Beverly S BS; Morrow, Bernice E BE; ,
Publication Date: 2017-10

Variant appearance in text: rs16869392
PubMed Link: 29025761
Variant Present in the following documents:
  • hcg-10-e001690-s001.pdf
View BVdb publication page