Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10149
Gene Symbol: ADGRG2
ADGRG2
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.010 Biomarker BEFREE To the best of our knowledge, these are the first two ADGRG2 variants to be identified in Chinese CBAVD patients, which further validate the disease-causing role of ADGRG2 in this congenital defect. 28805948

2017