ADGRV1 c.18433-19214A>G

Variant ID: 5-90426633-A-G

NM_032119.3(ADGRV1):c.18433-19214A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: rs2950858
PubMed Link: 29025761
Variant Present in the following documents:
  • hcg-10-e001690-s001.pdf
View BVdb publication page