Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907212
rs387907212
Entrez Id: 5885
Gene Symbol: RAD21
RAD21
CUI: C3553517
Disease:
CORNELIA DE LANGE SYNDROME 4
0.800 GeneticVariation UNIPROT RAD21 mutations cause a human cohesinopathy. 22633399 2012
dbSNP: rs387907212
rs387907212
Entrez Id: 5885
Gene Symbol: RAD21
RAD21
CUI: C3553517
Disease:
CORNELIA DE LANGE SYNDROME 4
C 0.800 CausalMutation CLINVAR RAD21 mutations cause a human cohesinopathy. 22633399 2012