Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs774488954
rs774488954
Entrez Id: 10149;101928415
Gene Symbol: ADGRG2;LOC101928415
ADGRG2;LOC101928415
CUI: C0403814
Disease:
Congenital bilateral aplasia of vas deferens
CA 0.700 CausalMutation CLINVAR Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens. 27476656 2016
dbSNP: rs879255538
rs879255538
Entrez Id: 10149;101928415
Gene Symbol: ADGRG2;LOC101928415
ADGRG2;LOC101928415
CUI: C0403814
Disease:
Congenital bilateral aplasia of vas deferens
C 0.700 CausalMutation CLINVAR Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens. 27476656 2016
dbSNP: rs879255539
rs879255539
Entrez Id: 10149;101928415
Gene Symbol: ADGRG2;LOC101928415
ADGRG2;LOC101928415
CUI: C0403814
Disease:
Congenital bilateral aplasia of vas deferens
TCT 0.700 CausalMutation CLINVAR Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens. 27476656 2016