Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11759064
rs11759064
PRKN ; LOC105369171
T 0.700 GeneticVariation GWASCAT Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux. 29097723

2017
dbSNP: rs527656756
rs527656756
HAAO ; MTA3
CA 0.700 CausalMutation CLINVAR NAD Deficiency, Congenital Malformations, and Niacin Supplementation. 28792876

2017
dbSNP: rs606231357
rs606231357
EYA1
T 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: rs1555883505
rs1555883505
EEF1A2
A 0.700 CausalMutation CLINVAR Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy. 26795593

2016
dbSNP: rs387907144
rs387907144
ARID1B
T 0.700 CausalMutation CLINVAR Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability. 26350204

2015
dbSNP: rs387907144
rs387907144
ARID1B
T 0.700 CausalMutation CLINVAR Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome. 22426309

2012
dbSNP: rs1057519521
rs1057519521
EBF3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1114167293
rs1114167293
C12orf57
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553553086
rs1553553086
FARSB
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554844486
rs1554844486
KAT6B
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555247805
rs1555247805
MED13L
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555955296
rs1555955296
CDKL5
T 0.700 CausalMutation CLINVAR

dbSNP: rs1556914274
rs1556914274
HUWE1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs200661329
rs200661329
PIGQ
A 0.700 GeneticVariation CLINVAR

dbSNP: rs796052505
rs796052505
GABRG2
A 0.700 CausalMutation CLINVAR

dbSNP: rs863223330
rs863223330
SIX1 ; MIR9718
G 0.700 GeneticVariation CLINVAR

dbSNP: rs875989802
rs875989802
DDX3X
A 0.700 GeneticVariation CLINVAR

dbSNP: rs5443
rs5443
GNB3 ; CDCA3
0.020 GeneticVariation BEFREE (2) TT genotype polymorphism rs5443 GNB3 gene may be a protective factor for the improved renal function in patients with primary vesicoureteral reflux in patients with genotype CC or CT. 27988909

2017
dbSNP: rs5443
rs5443
GNB3 ; CDCA3
0.020 GeneticVariation BEFREE G-protein beta3 subunit gene C825T polymorphism in patients with vesico-ureteric reflux. 15337465

2004
dbSNP: rs5186
rs5186
AGTR1
0.010 GeneticVariation BEFREE (1) No relationship was found between the studied polymorphisms (14094 ACE gene, rs1800469 gene TGFβ1, GNB3 gene rs5443, rs5186 AGTR1 gene) and the occurrence of primary vesicoureteral reflux. 27988909

2017
dbSNP: rs4073
rs4073
CXCL8
0.010 GeneticVariation BEFREE Following the elimination of vesicoureteral reflux, which is a significant risk factor for severe parenchymal infection, a single SNP in IL-8 (rs4073) was found to be associated with clinically severe ALN. 21042230

2011
dbSNP: rs1799939
rs1799939
RET
0.010 GeneticVariation BEFREE RET Gly691Ser mutation is associated with primary vesicoureteral reflux in the French-Canadian population from Quebec. 18273880

2008
dbSNP: rs1800469
rs1800469
TGFB1 ; B9D2
0.010 GeneticVariation BEFREE The aim of this study was to assess the association between the transforming growth factor-beta1 (TGF-beta1) gene polymorphisms rs1800469 (commonly known as T-509C) and rs1982073 (commonly known as Leu (10)-->Pro) and primary vesicoureteral reflux (VUR) and renal scarring. 18685869

2008
dbSNP: rs1982073
rs1982073
TGFB1
0.010 GeneticVariation BEFREE The aim of this study was to assess the association between the transforming growth factor-beta1 (TGF-beta1) gene polymorphisms rs1800469 (commonly known as T-509C) and rs1982073 (commonly known as Leu (10)-->Pro) and primary vesicoureteral reflux (VUR) and renal scarring. 18685869

2008