Gene: FAM149B1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 317662
Gene Symbol: FAM149B1
FAM149B1 		0.310 GeneticVariation disease BEFREE We subsequently identified a third Arab consanguineous multiplex family in which the phenotype of Joubert syndrome/oral-facial-digital syndrome (OFD VI) was found to co-segregate with the same founder variant in FAM149B1. 30905400 2019
Entrez Id: 317662
Gene Symbol: FAM149B1
FAM149B1 		0.310 Biomarker disease GENOMICS_ENGLAND We subsequently identified a third Arab consanguineous multiplex family in which the phenotype of Joubert syndrome/oral-facial-digital syndrome (OFD VI) was found to co-segregate with the same founder variant in FAM149B1. 30905400 2019