rs1211950654, CYP26B1

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital abnormal Synostosis
CUI: C0039093
Disease: Congenital abnormal Synostosis
0.010 GeneticVariation BEFREE This woman homozygous for c.1303G>A; p.(Gly435Ser) in CYP26B1, which was associated with multisutural synostosis, radiohumeral synostosis, normal bone mineral density, and apparent intellectual disability, a phenotype with significant similarities to Antley-Bixler and Pfeiffer syndromes.© 2016 Wiley Periodicals, Inc. 27410456 2016