Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909574
rs121909574
Entrez Id: 7020;109729173
Gene Symbol: TFAP2A;TFAP2A-AS2
TFAP2A;TFAP2A-AS2
CUI: C0000772
Disease:
Multiple congenital anomalies
A 0.700 GeneticVariation CLINVAR A clinical and molecular analysis of branchio-oculo-facial syndrome patients in Russia revealed new mutations in TFAP2A. 25590586 2015
dbSNP: rs121909574
rs121909574
Entrez Id: 7020;109729173
Gene Symbol: TFAP2A;TFAP2A-AS2
TFAP2A;TFAP2A-AS2
CUI: C0000772
Disease:
Multiple congenital anomalies
A 0.700 GeneticVariation CLINVAR Analysis of TFAP2A mutations in Branchio-Oculo-Facial Syndrome indicates functional complexity within the AP-2α DNA-binding domain. 23578821 2013
dbSNP: rs121909574
rs121909574
Entrez Id: 7020;109729173
Gene Symbol: TFAP2A;TFAP2A-AS2
TFAP2A;TFAP2A-AS2
CUI: C0000772
Disease:
Multiple congenital anomalies
A 0.700 GeneticVariation CLINVAR Genotype-phenotype analysis of the branchio-oculo-facial syndrome. 21204207 2011
dbSNP: rs121909574
rs121909574
Entrez Id: 7020;109729173
Gene Symbol: TFAP2A;TFAP2A-AS2
TFAP2A;TFAP2A-AS2
CUI: C0000772
Disease:
Multiple congenital anomalies
A 0.700 GeneticVariation CLINVAR Additional clinical and molecular analyses of TFAP2A in patients with the branchio-oculo-facial syndrome. 20358615 2010
dbSNP: rs121909574
rs121909574
Entrez Id: 7020;109729173
Gene Symbol: TFAP2A;TFAP2A-AS2
TFAP2A;TFAP2A-AS2
CUI: C0000772
Disease:
Multiple congenital anomalies
A 0.700 GeneticVariation CLINVAR Confirmation of TFAP2A gene involvement in branchio-oculo-facial syndrome (BOFS) and report of temporal bone anomalies. 19764023 2009
dbSNP: rs121909574
rs121909574
Entrez Id: 7020;109729173
Gene Symbol: TFAP2A;TFAP2A-AS2
TFAP2A;TFAP2A-AS2
CUI: C0000772
Disease:
Multiple congenital anomalies
A 0.700 GeneticVariation CLINVAR Further delineation of the branchio-oculo-facial syndrome. 7747785 1995