Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519371
rs1057519371
HNF1B ; LOC105371754
TG 0.700 CausalMutation CLINVAR Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene. 27657687

2017
dbSNP: rs1555202126
rs1555202126
CEP290
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555454847
rs1555454847
PKD1
G 0.700 CausalMutation CLINVAR

dbSNP: rs376493409
rs376493409
CEP290
A 0.700 CausalMutation CLINVAR