Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs766132877
rs766132877
Entrez Id: 79809
Gene Symbol: TTC21B
TTC21B
CUI: C1865872
Disease:
NEPHRONOPHTHISIS 2
C 0.700 CausalMutation CLINVAR