Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4849121
rs4849121
G 0.800 GeneticVariation GWASCAT A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy. 22197929

2011

dbSNP: rs6677604
rs6677604
CFH
0.750 GeneticVariation BEFREE Moreover, rs6677604 might contribute to the difference of complement activation intensity between IgAVN and IgAN. 30838755

2020

dbSNP: rs6677604
rs6677604
CFH
0.750 GeneticVariation BEFREE We found both rs800292-GG and rs6677604-GG were risk genotypes for complement activation in IgAN patients, as represented by lower plasma C3 levels in IgAN patients with rs800292-GG and a higher intensity of glomerular C3 deposits in those with rs6677604-GG, respectively. 30219152

2018

dbSNP: rs6677604
rs6677604
CFH
0.750 GeneticVariation BEFREE Our pooled analysis showed a significant association between rs6677604-(A) allele and Ig</span>AN susceptibility, supporting the importance of complement activation in the pathogenesis of IgAN. 29240274

2018

dbSNP: rs6677604
rs6677604
CFH
0.750 GeneticVariation BEFREE The CFHR3,1Δ and rs6677604-A alleles were rare (4.4% in patients and 7.1% in controls) and in strong linkage disequilibrium with each other (r<sup>2</sup>=0.95); of these alleles, CFHR3,1Δ associated more significantly with decreased risk of IgAN (odds ratio [OR], 0.56; 95% confidence interval [95% CI], 0.46 to 0.70; P=8.5 × 10<sup>-8</sup> versus OR, 0.61; 95% CI, 0.50 to 0.75; P=1.6 × 10<sup>-6</sup> for rs6677604-A). 26940089

2016

dbSNP: rs6677604
rs6677604
CFH
0.750 GeneticVariation BEFREE Our recent genome-wide association study of IgAN identified susceptibility loci on 1q32 containing the complement regulatory protein-encoding genes CFH and CFHR1-5, with rs6677604 in CFH as the top single-nucleotide polymorphism and CFHR3-1 deletion (CFHR3-1∆) as the top signal for copy number variation. 25205734

2015

dbSNP: rs6677604
rs6677604
CFH
G 0.750 GeneticVariation GWASCAT Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. 25305756

2014

dbSNP: rs11264799
rs11264799
0.720 GeneticVariation BEFREE Moreover, the haplotypes ACC (p = 0.02) and CTC (p = 0.017) of LD block rs11264794/rs7522061/rs11264799 in the FCRL3 gene were significantly associated with a decreased risk of IgAN. 31780315

2020

dbSNP: rs11264799
rs11264799
0.720 GeneticVariation BEFREE We found that four SNPs (rs11264794, rs7865684, rs11264799, and rs6691569) were significantly associated with IgAN susceptibility after Bonferroni correction in the combined samples. 31433201

2019

dbSNP: rs9275596
rs9275596
0.720 GeneticVariation BEFREE After Cochran-Armitage test for trend analysis, seven IgAN-associated SNPs located in the major histocompatibility complex (MHC) region were found to be significantly associated with the susceptibility of IMN, with rs9275596 as the top one (p = 1.97E-43, OR = 3.977). 28929317

2017

dbSNP: rs9275596
rs9275596
0.720 GeneticVariation BEFREE The T allele at rs9275596 was significantly associated with macroscopic haematuria of IgAN patients under the dominant and additive models of inheritance, (P < 0.001, Pc = 0.007, OR = 2.983) and (P < 0.001, Pc = 0.007, OR = 2.17), respectively. 27450519

2017

dbSNP: rs9275596
rs9275596
0.720 GeneticVariation BEFREE A combination of the rs2856717T/C, rs9275596C/T, and rs2412971A/G had effects on the susceptibility of IgAN (P = 0.001). 27450519

2017

dbSNP: rs11264799
rs11264799
C 0.720 GeneticVariation GWASCAT Identification of new susceptibility loci for IgA nephropathy in Han Chinese. 26028593

2015

dbSNP: rs9275596
rs9275596
T 0.720 GeneticVariation GWASCAT Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. 25305756

2014

dbSNP: rs7190997
rs7190997
0.710 GeneticVariation BEFREE We found that four SNPs (rs11150619, rs11150614, rs7190997, and rs4597342) showed potential associations with IgAN susceptibility in the discovery stage, but only SNP rs11150619 was further genotyped in the validation stage after multiple testing. 31227791

2019

dbSNP: rs17019602
rs17019602
0.710 GeneticVariation BEFREE In comparison, neither rs4077515 nor rs17019602 showed significant association between genotype distribution and clinical parameters in IgAN patients (<i>P</i> > 0.05). 29100328

2017

dbSNP: rs2412971
rs2412971
0.710 GeneticVariation BEFREE A combination of the rs2856717T/C, rs9275596C/T, and rs2412971A/G had effects on the susceptibility of IgAN (P = 0.001). 27450519

2017

dbSNP: rs2856717
rs2856717
0.710 GeneticVariation BEFREE A combination of the rs2856717T/C, rs9275596C/T, and rs2412971A/G had effects on the susceptibility of IgAN (P = 0.001). 27450519

2017

dbSNP: rs2856717
rs2856717
0.710 GeneticVariation BEFREE rs2856717 may influence the clinical characteristics and poor outcome of IgAN. 27450519

2017

dbSNP: rs4077515
rs4077515
0.710 GeneticVariation BEFREE For additive interaction, the CT or TT of rs</span>4077515 and GG of 17019602 genotype combination conferred a 2.56-fold risk of IgAN reference to CC of 4077515 and AA of 17019602 (OR = 2.56, 95% CI: 0.98-6.69, <i>P</i> = 0.049). 29100328

2017

dbSNP: rs12716641
rs12716641
T 0.710 GeneticVariation GWASCAT Identification of new susceptibility loci for IgA nephropathy in Han Chinese. 26028593

2015

dbSNP: rs2738058
rs2738058
T 0.710 GeneticVariation GWASCAT Identification of new susceptibility loci for IgA nephropathy in Han Chinese. 26028593

2015

dbSNP: rs7190997
rs7190997
C 0.710 GeneticVariation GWASCAT Identification of new susceptibility loci for IgA nephropathy in Han Chinese. 26028593

2015

dbSNP: rs12716641
rs12716641
0.710 GeneticVariation BEFREE We found seven SNPs within DEFA genes that were significantly associated with IgAN, including rs2738048 discovered in our previous GWAS (p = 0.0007, OR = 0.77) and additional 6 SNPs (rs2615787, p = 0.0001, OR = 0.74; rs2738081, p = 0.0003, OR = 0.72; rs2738058, p = 0.0001, OR = 0.73; rs4288398, p = 0.0008, OR = 0.78; rs6984215, p = 0.002, OR = 0.63; rs12716641, p = 0.00002, OR = 0.71). 25024040

2014

dbSNP: rs17019602
rs17019602
G 0.710 GeneticVariation GWASCAT Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. 25305756

2014