Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200287952
rs200287952
COL4A3 ; MFF-DT
A 0.700 GeneticVariation GWASCAT Sequence variants associating with urinary biomarkers. 30476138

2019
dbSNP: rs56254331
rs56254331
TGFB1 ; CCDC97
A 0.700 GeneticVariation GWASCAT Sequence variants associating with urinary biomarkers. 30476138

2019
dbSNP: rs760545501
rs760545501 		T 0.700 GeneticVariation GWASCAT Sequence variants associating with urinary biomarkers. 30476138

2019
dbSNP: rs1441937959
rs1441937959
EFL1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1556411578
rs1556411578
COL4A5
T 0.700 CausalMutation CLINVAR

dbSNP: rs1556463583
rs1556463583
COL4A5
CA 0.700 GeneticVariation CLINVAR

dbSNP: rs1559643753
rs1559643753
COL4A4
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1569497030
rs1569497030
COL4A5
G 0.700 CausalMutation CLINVAR

dbSNP: rs199469465
rs199469465
SRCAP
T 0.700 CausalMutation CLINVAR

dbSNP: rs533297350
rs533297350
COL4A4
T 0.700 GeneticVariation CLINVAR

dbSNP: rs569681869
rs569681869
COL4A4
G 0.700 GeneticVariation CLINVAR

dbSNP: rs779593707
rs779593707
CLCNKB
CAATA 0.700 GeneticVariation CLINVAR

dbSNP: rs10969913
rs10969913 		0.010 GeneticVariation BEFREE Meta-analysis of the European ancestry cohorts identified three genomic signals: single nucleotide polymorphism (SNP) rs17055178 with rectal bleeding (Pmeta=6.2x10-10), rs10969913 with decreased urinary stream (Pmeta=2.9x10-10) and rs11122573 with hematuria (Pmeta=1.8x10-8). 31095341

2020
dbSNP: rs11122573
rs11122573 		0.010 GeneticVariation BEFREE Meta-analysis of the European ancestry cohorts identified three genomic signals: single nucleotide polymorphism (SNP) rs17055178 with rectal bleeding (Pmeta=6.2x10-10), rs10969913 with decreased urinary stream (Pmeta=2.9x10-10) and rs11122573 with hematuria (Pmeta=1.8x10-8). 31095341

2020
dbSNP: rs147121532
rs147121532
PGBD5
0.010 GeneticVariation BEFREE Fine scale mapping of these three regions identified another independent signal (rs147121532) associated with hematuria (Pconditional=4.7x10-6). 31095341

2020
dbSNP: rs17055178
rs17055178 		0.010 GeneticVariation BEFREE Meta-analysis of the European ancestry cohorts identified three genomic signals: single nucleotide polymorphism (SNP) rs17055178 with rectal bleeding (Pmeta=6.2x10-10), rs10969913 with decreased urinary stream (Pmeta=2.9x10-10) and rs11122573 with hematuria (Pmeta=1.8x10-8). 31095341

2020
dbSNP: rs121909585
rs121909585
C3
0.010 GeneticVariation BEFREE Homozygous C3 p.D1115N (C3KI) mice developed spontaneous chronic thrombotic microangiopathy together with hematuria, thrombocytopenia, elevated creatinine, and evidence of hemolysis. 30714990

2019
dbSNP: rs398123643
rs398123643
COL6A1
0.010 GeneticVariation BEFREE We report a 14-year-old boy who had both Bethlem myopathy and recurrent hematuria and who carried a known de novo COL6A1 missense mutation c.877G > A (p.G293R). 30808312

2019
dbSNP: rs761310536
rs761310536
COL6A2
0.010 GeneticVariation BEFREE We report a 14-year-old boy who had both Bethlem myopathy and recurrent hematuria and who carried a known de novo COL6A1 missense mutation c.877G > A (p.G293R). 30808312

2019
dbSNP: rs9644778
rs9644778 		0.010 GeneticVariation BEFREE Besides, marginally significant association of rs9644778 risk genotype with lower proportion of gross hematuria (CC+CA vs AA 35.2% vs 30.2%, P=0.073) was observed. 25675412

2016
dbSNP: rs1695
rs1695
GSTP1
0.010 GeneticVariation BEFREE In addition, patients with the GSTP1 rs1695 AA genotype had an increased risk of irritative voiding symptoms; while patients with the GSTO1 rs4925 CC genotype had a decreased risk of hematuria. 26354850

2015
dbSNP: rs2277798
rs2277798
UBASH3A
0.010 GeneticVariation BEFREE Moreover, we found that the genotype distribution of rs2277798 was significantly associated with hematuria in the SLE patients (p=0.003). 25843625

2015
dbSNP: rs4925
rs4925
GSTO1
0.010 GeneticVariation BEFREE In addition, patients with the GSTP1 rs1695 AA genotype had an increased risk of irritative voiding symptoms; while patients with the GSTO1 rs4925 CC genotype had a decreased risk of hematuria. 26354850

2015
dbSNP: rs12118043
rs12118043
FCGR2B
0.010 GeneticVariation BEFREE Associations between FCGR2B rs12118043 and proteinuria (p = 3.65×10(-2)) as well as gross hematuria (p = 4.53×10(-2)), between FCRLB rs4657093 and levels of serum creatinine (p = 2.67×10(-2)) as well as eGFR (p = 5.41*10(-3)) were also observed. 23593433

2013
dbSNP: rs4657093
rs4657093
FCRLB
0.010 GeneticVariation BEFREE Associations between FCGR2B rs12118043 and proteinuria (p = 3.65×10(-2)) as well as gross hematuria (p = 4.53×10(-2)), between FCRLB rs4657093 and levels of serum creatinine (p = 2.67×10(-2)) as well as eGFR (p = 5.41*10(-3)) were also observed. 23593433

2013