Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Nephritis, Interstitial
CUI: C0027707
Disease: Nephritis, Interstitial
0.010 GeneticVariation BEFREE Our results confirm the causal role of the homozygous p.P209L TTC21B mutation in two new families with FSGS and tubulointerstitial disease. 26940125 2017