Disease: OROFACIODIGITAL SYNDROME XIV ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777653
rs587777653
Entrez Id: 26005
Gene Symbol: C2CD3
C2CD3
CUI: C4014780
Disease:
OROFACIODIGITAL SYNDROME XIV 		A 0.700 CausalMutation CLINVAR