Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 100506134
Gene Symbol: TTC21B-AS1
TTC21B-AS1
0.100 CausalMutation disease CLINVAR A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS. 24876116 2014
Entrez Id: 100506134
Gene Symbol: TTC21B-AS1
TTC21B-AS1
0.100 CausalMutation disease CLINVAR TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum. 21258341 2011
Entrez Id: 100506134
Gene Symbol: TTC21B-AS1
TTC21B-AS1
0.100 GeneticVariation disease CLINVAR