Disease: Cockayne Syndrome, Type II ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906262
rs387906262
Entrez Id: 2074;267004
Gene Symbol: ERCC6;PGBD3
ERCC6;PGBD3
CUI: C0751038
Disease:
Cockayne Syndrome, Type II 		CT 0.700 CausalMutation CLINVAR