Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1561964103
rs1561964103
Entrez Id: 7021
Gene Symbol: TFAP2B
TFAP2B
CUI: C1868570
Disease:
CHAR SYNDROME
C 0.700 CausalMutation CLINVAR