Gene: BBS2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 583
Gene Symbol: BBS2
BBS2 		0.020 GeneticVariation group BEFREE Here, we report the identification of a founder mutation in the BBS2 gene as the cause for the increased incidence of this developmental disorder in the Hutterite population. 20618352 2010
Entrez Id: 583
Gene Symbol: BBS2
BBS2 		0.020 Biomarker group BEFREE Bardet-Biedl syndrome (BBS: OMIM 209900) is a rare developmental disorder that exhibits significant clinical and genetic heterogeneity. 14976158 2004