Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6068020
rs6068020
0.800 GeneticVariation GWASDB Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. 19478329

2010

dbSNP: rs6068020
rs6068020
0.800 GeneticVariation GWASCAT Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. 19478329

2010

dbSNP: rs9814870
rs9814870
0.800 GeneticVariation GWASCAT Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. 19478329

2010

dbSNP: rs9814870
rs9814870
0.800 GeneticVariation GWASDB Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. 19478329

2010

dbSNP: rs10966811
rs10966811
0.010 GeneticVariation BEFREE In this study, we investigated whether the rs10966811 (located in an intergenic region between the TUSC1 and IZUMO3 genes) and rs10129954 (located in the DPF3 gene) SNPs, previously related to family size, are associated with male infertility. 28975488

2018

dbSNP: rs12097821
rs12097821
0.010 GeneticVariation BEFREE The results suggested that rs2477686, rs6080550, and rs10842262 were significantly associated with male infertility, especially with NOA, while rs12097821 was only found to be associated with total male infertility. 30863997

2019

dbSNP: rs1259503
rs1259503
0.010 GeneticVariation BEFREE Moreover, we could not find any differences in the variants rs7896741 and rs1259503, which showed no risk of male infertility, whether normal or abnormal. 27806320

2016

dbSNP: rs6476866
rs6476866
0.010 GeneticVariation BEFREE A total of 136 subfertile men and 456 healthy fertile men were recruited. rs6476866 in SLC1A1 (P = 1.919E-4, OR = 0.5905, 95% CI: 0.447-0.78) and rs10129954 in DPF3 (P = 0.0023, OR = 2.199, 95% CI: 1.311-3.689) were strongly associated with idiopathic male infertility. 27232852

2018

dbSNP: rs724078
rs724078
0.010 GeneticVariation BEFREE Are the four candidate loci (rs7867029, rs7174015, rs12870438 and rs724078) for human male fertility traits, identified in a genome-wide association study (GWAS) of a Hutterite population in the USA, associated with male infertility in a Japanese population? 25908656

2015

dbSNP: rs727428
rs727428
0.010 GeneticVariation BEFREE Also, genotype frequencies, allele frequency, and haplotype were all analyzed in both groups.There were statistical differences in A allele frequency (P = .017) and GA genotype frequency (P = .016) of SHBG gene rs6259 locus and in CC genotype frequency of SHBG gene rs727428 locus (P = .034) between the 2 groups.Male infertility is associated with GA genotype and A allele of rs6259 locus, as well as CC genotype of rs727428 locus in SHBG gene. 28796064

2017

dbSNP: rs1045642
rs1045642
0.010 GeneticVariation BEFREE Association of the MDR1 (ABCB1) gene 3435C>T polymorphism with male infertility. 19815951

2010

dbSNP: rs2066853
rs2066853
AHR
0.040 GeneticVariation BEFREE To examine whether Arg554Lys polymorphism in the gene for aryl hydrocarbon receptor (AHR) and/or Pro185Ala polymorphism in the gene for aryl hydrocarbon receptor repressor (AHRR) constitutes a susceptibility locus for dioxin-related male infertility. 15474075

2004

dbSNP: rs2066853
rs2066853
AHR
0.040 GeneticVariation BEFREE The pooled results showed that there was no significant association between <i>AHR</i> rs2066853</span> gene polymorphism and male infertility risk (A vs. G: OR = 1.08, 95% CI = 0.83-1.39; AA vs. GG: OR = 1.16, 95% CI = 0.65-2.04; AA vs. GA + GG: OR = 1.17, 95% CI = 0.66-2.07; AA + GA vs. GG: OR = 0.99, 95% CI = 0.85-1.15). 31662023

2019

dbSNP: rs2066853
rs2066853
AHR
0.040 GeneticVariation BEFREE Homozygosity for the rs2066853 A allele and rs2282885 C allele decreases and increases the risk of developing male infertility, respectively. 23703535

2013

dbSNP: rs2066853
rs2066853
AHR
0.040 GeneticVariation BEFREE Subgroup analysis by study population revealed there was no association between AhR Arg554Lys polymorphism and susceptibility to male infertility in Asian population (G versus A, OR (95%CI) = 1.099 (0.940-1.286); GG vs AA, OR (95%CI) = 0.982 (0.781-1.235); GA versus AA, OR (95%CI) = 1.220 (0.726-2.052); GG + GA vs AA, OR (95%CI) = 1.221 (0.740-1.982); GG versus GA + AA, OR (95%CI) = 1.087 (0.919-1.286)). 29427904

2018

dbSNP: rs2282885
rs2282885
AHR
0.010 GeneticVariation BEFREE Homozygosity for the rs2066853 A allele and rs2282885 C allele decreases and increases the risk of developing male infertility, respectively. 23703535

2013

dbSNP: rs2292596
rs2292596
0.020 GeneticVariation BEFREE The Pro185Ala polymorphism in AHRR may constitute a susceptibility locus for dioxin-related male infertility. 15474075

2004

dbSNP: rs2292596
rs2292596
0.020 GeneticVariation BEFREE We found that polymorphism rs2292596 (Pro185Ala) was statistically significantly associated with the risk of male infertility. 30506768

2019

dbSNP: rs116298211
rs116298211
AK7
0.010 GeneticVariation BEFREE Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia. 29365104

2018

dbSNP: rs1262199907
rs1262199907
AR
0.010 GeneticVariation BEFREE To this aim, we selected four AR missense mutations associated with isolated male infertility (L547F and two novel mutations A474V and S650G) or partial AIS (Y571H). 17970778

2008

dbSNP: rs139524801
rs139524801
AR
0.010 GeneticVariation BEFREE To this aim, we selected four AR missense mutations associated with isolated male infertility (L547F and two novel mutations A474V and S650G) or partial AIS (Y571H). 17970778

2008

dbSNP: rs141425171
rs141425171
AR
0.010 GeneticVariation BEFREE A novel mutation (N233K) in the transactivating domain and the N756S mutation in the ligand binding domain of the androgen receptor gene are associated with male infertility. 11422119

2001

dbSNP: rs200390780
rs200390780
AR
0.010 GeneticVariation BEFREE To this aim, we selected four AR missense mutations associated with isolated male infertility (L547F and two novel mutations A474V and S650G) or partial AIS (Y571H). 17970778

2008

dbSNP: rs952566855
rs952566855
ATM
0.010 GeneticVariation BEFREE In addition, the homozygous variant genotype GG of RAG1 rs2227973 (A>G, K820R) was associated with a significantly increased risk of male infertility (adjusted OR, 1.44; 95% CI, 1.01-2.04). 23630330

2013

dbSNP: rs140027779
rs140027779
0.010 GeneticVariation BEFREE No association of the A260G and A386G DAZL single nucleotide polymorphisms with male infertility in a Caucasian population. 15520024

2004