Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1203334353
rs1203334353
0.010 GeneticVariation BEFREE Two variants, c.671A>G (p.(Asn224Ser)) in DMRT1 and c.91C>T (p.(Arg31Cys)) in REC8, have already been described in association with azoospermia. 31479588

2020

dbSNP: rs140506267
rs140506267
0.010 GeneticVariation BEFREE Two variants, c.671A>G (p.(Asn224Ser)) in DMRT1 and c.91C>T (p.(Arg31Cys)) in REC8, have already been described in association with azoospermia. 31479588

2020

dbSNP: rs140506267
rs140506267
0.010 GeneticVariation BEFREE Two variants, c.671A>G (p.(Asn224Ser)) in DMRT1 and c.91C>T (p.(Arg31Cys)) in REC8, have already been described in association with azoospermia. 31479588

2020

dbSNP: rs34075659
rs34075659
0.010 GeneticVariation BEFREE Two variants, c.671A>G (p.(Asn224Ser)) in DMRT1 and c.91C>T (p.(Arg31Cys)) in REC8, have already been described in association with azoospermia. 31479588

2020

dbSNP: rs150771661
rs150771661
0.010 GeneticVariation BEFREE Our early studies revealed a missense mutation (R242H) of GRTH in 5.8% of Japanese patient population with azoospermia. 31040297

2019

dbSNP: rs26279
rs26279
0.010 GeneticVariation BEFREE The genotype frequency distribution of rs26279 (A>G) in MSH3 was found to be significantly different between IMI and control (p < 0.05), as well as azoospermia. 31342644

2019

dbSNP: rs6166
rs6166
0.010 GeneticVariation BEFREE We evaluated the association of the single-nucleotide polymorphisms (SNP) FSHB -211G>T (rs10835638), FSHR -29G>A (rs1394205), and FSHR c.2039A>G (rs6166) with testicular histopathology and SRR in patients with azoospermia. 30668782

2019

dbSNP: rs10129954
rs10129954
0.010 GeneticVariation BEFREE Also, a statistically significant association between rs10129954 and azoospermia, and oligozoospermia was observed. 28975488

2018

dbSNP: rs11531577
rs11531577
0.010 GeneticVariation BEFREE No significant differences in allele and genotype frequencies of SNP rs1050482 and rs11531577 in STAG3 gene as well as rs2288846 in RFX2 gene between patients with azoospermia and controls were observed. 29277047

2018

dbSNP: rs12348
rs12348
0.010 GeneticVariation BEFREE When we assessed the relationship between rs12348 in TUSC1 and rs2772579 in IZUMO3 and male infertility traits, we found that rs12348 in TUSC1 was significantly associated with azoospermia and oligozoospermia, but rs2772579 in IZUMO3 was not associated with male infertility. 28975488

2018

dbSNP: rs2070744
rs2070744
0.010 GeneticVariation BEFREE The aim of this study was to assess the possible association of three genetic variants (rs2070744, rs1799983 and intron variant 4a/4b) in NOS3 gene and infertility occurrence in two groups of infertile men (idiopathic azoospermia and oligoasthenozoospermia) and fertile controls. 28466478

2018

dbSNP: rs2288846
rs2288846
0.010 GeneticVariation BEFREE No significant differences in allele and genotype frequencies of SNP rs1050482 and rs11531577 in STAG3 gene as well as rs2288846 in RFX2 gene between patients with azoospermia and controls were observed. 29277047

2018

dbSNP: rs4045481
rs4045481
0.010 GeneticVariation BEFREE The polymorphism of SNP rs4045481 in RNF212 gene might be associated with azoospermia and genotype CC of this SNP may be a risk factor of azoospermia. 29277047

2018

dbSNP: rs68073206
rs68073206
0.010 GeneticVariation BEFREE We addressed the functional consequences of SNP rs68073206, located at the +5 position of an alternative 5' splice donor site, and observed its association with male infertility in the subjects with azoospermia, oligoasthenozoospermia and normozoospermia. 28367994

2017

dbSNP: rs11614913
rs11614913
0.010 GeneticVariation BEFREE In following stratified analysis, we found that rs11614913 exhibited a significantly higher risk of asthenospermia, oligozoospermia and azoospermia. 26805933

2016

dbSNP: rs222859
rs222859
0.010 GeneticVariation BEFREE Association of G/T(rs222859) polymorphism in Exon 1 of YBX2 gene with azoospermia, among Iranian infertile males. 26804374

2016

dbSNP: rs11204546
rs11204546
0.010 GeneticVariation BEFREE Clinically, the SNPs (rs11204546 of OR2W3 and rs11677854 of GTF2A1L ) might be additional valuable molecular predictive markers for assessing the treatment of NOA patients. 25374392

2015

dbSNP: rs11677854
rs11677854
0.010 GeneticVariation BEFREE Clinically, the SNPs (rs11204546 of OR2W3 and rs11677854 of GTF2A1L ) might be additional valuable molecular predictive markers for assessing the treatment of NOA patients. 25374392

2015

dbSNP: rs1335054067
rs1335054067
0.010 GeneticVariation BEFREE This novel mutation (p. V385L) of DAX-1 is the first to be identified in association with secretory azoospermia, thereby highlighting the important role of DAX-1 in spermatogenesis. 26207377

2015

dbSNP: rs1801394
rs1801394
0.010 GeneticVariation BEFREE The polymorphic distributions of the four SNPs (MTHFR C677T and A1298C, MTR A2756G and MTRR A66G) were investigated by the method of SNaPshot in a Chinese cohort including 296 idiopathic infertile males with azoospermia or oligozoospermia and 204 fertile males. 25578539

2015

dbSNP: rs1805087
rs1805087
MTR
0.010 GeneticVariation BEFREE The polymorphic distributions of the four SNPs (MTHFR C677T and A1298C, MTR A2756G and MTRR A66G) were investigated by the method of SNaPshot in a Chinese cohort including 296 idiopathic infertile males with azoospermia or oligozoospermia and 204 fertile males. 25578539

2015

dbSNP: rs55763075
rs55763075
0.010 GeneticVariation BEFREE Our results indicated that the MTHFR 3'-UTR rs55763075 polymorphism might modify the susceptibility to male infertility with idiopathic azoospermia. 26505368

2015

dbSNP: rs724078
rs724078
0.010 GeneticVariation BEFREE There were no associations between rs724078 and azoospermia or oligozoospermia. 25908656

2015

dbSNP: rs769642496
rs769642496
0.010 GeneticVariation BEFREE 1) A novel variant in exon 1 (p.Pro130Leu) that disrupted a mammalian specific polyproline stretch in the self-association domain was more frequent in azoospermia cases (0.27% vs 0.13%, p = 0.549). 25451826

2015

dbSNP: rs7867029
rs7867029
0.010 GeneticVariation BEFREE The SNPs rs7867029 and rs7174015 are associated with oligozoospermia [rs7867029: odds ratio (OR) = 1.70, 95% confidence interval (CI) = 1.07-2.68, P = 0.024 (log-additive); rs7174015: OR = 6.52, 95% CI = 1.57-27.10, P = 0.0099 (dominant)] and rs12870438 is associated with azoospermia (OR = 10.90, 95% CI = 2.67-44.60, P = 0.00087 (recessive)] and oligozoospermia [OR = 8.54, 95% CI = 1.52-47.90, P = 0.015 (recessive)]. 25908656

2015