TTC21B, tetratricopeptide repeat domain 21B, 79809

N. diseases: 76; N. variants: 24
Disease: NEPHRONOPHTHISIS 12 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs146320075
rs146320075
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B
CUI: C3151186
Disease:
NEPHRONOPHTHISIS 12 		0.700 GeneticVariation UNIPROT TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum. 21258341 2011