Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886037856
rs886037856
Entrez Id: 727857
Gene Symbol: BHLHA9
BHLHA9
CUI: C1843758
Disease:
Camptosynpolydactyly, Complex
0.800 GeneticVariation UNIPROT Complex Camptosynpolydactyly and Mesoaxial synostotic syndactyly with phalangeal reduction are allelic disorders. 27041388 2016
dbSNP: rs886037856
rs886037856
Entrez Id: 727857
Gene Symbol: BHLHA9
BHLHA9
CUI: C1843758
Disease:
Camptosynpolydactyly, Complex
TT 0.800 GeneticVariation CLINVAR