Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200750564
rs200750564
T 0.700 CausalMutation CLINVAR

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE Our meta-analysis showed that the MTHFR C677T mutation was a risk factor for male infertility in both azoospermia and oligoasthenoteratozoospermia patients, especially in Asian population. 26549413

2015

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE Influence of methylenetetrahydrofolate reductase C677T gene polymorphisms in Algerian infertile men with azoospermia or severe oligozoospermia. 22928696

2012

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE The objective of this study was to analyze the distribution of the methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms in idiopathic infertile Brazilian patients with nonobstructive azoospermia (NOA) or severe oligozoospermia and fertile Brazilian men as controls to explore the possible association of these polymorphisms and male infertility. 21138341

2011

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE Single nucleotide polymorphism C677T in the methylenetetrahydrofolate reductase gene might be a genetic risk factor for infertility for Chinese men with azoospermia or severe oligozoospermia. 16888682

2007

dbSNP: rs397507444
rs397507444
0.030 GeneticVariation BEFREE Pooled estimate on c.1298A>C data from all published studies including our data showed no association of this polymorphism with male infertility (Odds ratio = 1.035, P = 0.56), azoospermia (Odds ratio = 0.97, P = 0.74), or oligoasthenoteratozoospermia (Odds ratio = 0.92, p = 0.29). 23874907

2013

dbSNP: rs397507444
rs397507444
0.030 GeneticVariation BEFREE However, the homozygous (C/C) A1298C polymorphism of the MTHFR gene was present at a statistically high significance in severe oligozoospermia group compared with controls (OR = 3.372, 95% confidence interval CI = 1.27-8.238; p = 0.01431). 22457816

2012

dbSNP: rs397507444
rs397507444
0.030 GeneticVariation BEFREE The objective of this study was to analyze the distribution of the methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms in idiopathic infertile Brazilian patients with nonobstructive azoospermia (NOA) or severe oligozoospermia and fertile Brazilian men as controls to explore the possible association of these polymorphisms and male infertility. 21138341

2011

dbSNP: rs4647269
rs4647269
0.020 GeneticVariation BEFREE The rs1800734 and rs4647269 in MLH1 were found to be significantly different between severe oligozoospermia and control groups (p < 0.05). 31342644

2019

dbSNP: rs12870438
rs12870438
0.020 GeneticVariation BEFREE Of these, three SNPs (rs7867029, rs7174015, and rs12870438) were found to be significantly associated with the risk of azoospermia and/or oligozoospermia in a Japanese population. 28975488

2018

dbSNP: rs7174015
rs7174015
0.020 GeneticVariation BEFREE Of these, three SNPs (rs7867029, rs7174015, and rs12870438) were found to be significantly associated with the risk of azoospermia and/or oligozoospermia in a Japanese population. 28975488

2018

dbSNP: rs12870438
rs12870438
0.020 GeneticVariation BEFREE The association between rs7174015 and oligozoospermia under a dominant model and between rs12870438 and azoospermia under additive and recessive models remained after correction for multiple testing. 25908656

2015

dbSNP: rs7174015
rs7174015
0.020 GeneticVariation BEFREE The association between rs7174015 and oligozoospermia under a dominant model and between rs12870438 and azoospermia under additive and recessive models remained after correction for multiple testing. 25908656

2015

dbSNP: rs2075789
rs2075789
0.020 GeneticVariation BEFREE One intronic SNP in MLH1 (rs4647269) and two non-synonymous SNPs in PMS2 (rs1059060, Ser775Asn) and MSH5 (rs2075789, Pro29Ser) seem to be risk factors for the development of azoospermia or oligozoospermia. 22594646

2012

dbSNP: rs4647269
rs4647269
0.020 GeneticVariation BEFREE One intronic SNP in MLH1 (rs4647269) and two non-synonymous SNPs in PMS2 (rs1059060, Ser775Asn) and MSH5 (rs2075789, Pro29Ser) seem to be risk factors for the development of azoospermia or oligozoospermia. 22594646

2012

dbSNP: rs6166
rs6166
0.020 GeneticVariation BEFREE In this study, we have evaluated the response of FSH treatment in terms of sperm production on the basis of Ala307Thr-Asn680Ser polymorphisms in the FSHR gene in a group of oligozoospermic subjects with hypospermatogenesis and normal FSH levels. 20569270

2011

dbSNP: rs2075789
rs2075789
0.020 GeneticVariation BEFREE The role of MSH5 C85T and MLH3 C2531T polymorphisms in the risk of male infertility with azoospermia or severe oligozoospermia. 19808033

2010

dbSNP: rs6166
rs6166
0.020 GeneticVariation BEFREE In the present study, the common G-29A, A919G, and A2039G polymorphisms in the FSHR gene were analysed in 150 (36 non-obstructive azoospermia and 114 individuals with oligozoospermia) patients and 208 normozoospermic men. 20170288

2010

dbSNP: rs121918346
rs121918346
0.020 GeneticVariation BEFREE Our results show that the T54A polymorphism in DAZL has no major role in Japanese males with azoospermia or oligozoospermia. 16123080

2005

dbSNP: rs121918346
rs121918346
0.020 GeneticVariation BEFREE The phenotypes varied significantly in cases with heterozygous T54A polymorphism, ranging from hypospermatogenesis and maturation arrest to Sertoli cell-only syndrome. 12414900

2002

dbSNP: rs10842262
rs10842262
0.010 GeneticVariation BEFREE The results showed that rs12097821 and rs10842262 were strongly associated with the risk of NOA but not total male infertility or oligozoospermia, while rs2477686 and rs6080550 were not associated with the risk of total male infertility, NOA, or oligozoospermia. 30863997

2019

dbSNP: rs1800734
rs1800734
0.010 GeneticVariation BEFREE The rs1800734 and rs4647269 in MLH1 were found to be significantly different between severe oligozoospermia and control groups (p < 0.05). 31342644

2019

dbSNP: rs2477686
rs2477686
0.010 GeneticVariation BEFREE The results showed that rs12097821 and rs10842262 were strongly associated with the risk of NOA but not total male infertility or oligozoospermia, while rs2477686 and rs6080550 were not associated with the risk of total male infertility, NOA, or oligozoospermia. 30863997

2019

dbSNP: rs2656927
rs2656927
0.010 GeneticVariation BEFREE Interestingly, the genotype frequencies of SNP rs2656927 (P = 0.014) and rs8103849 (P < 0.001) significantly differed between men with oligozoospermia in case group 1 and normozoospermic men. 31802345

2019

dbSNP: rs6080550
rs6080550
0.010 GeneticVariation BEFREE The results showed that rs12097821 and rs10842262 were strongly associated with the risk of NOA but not total male infertility or oligozoospermia, while rs2477686 and rs6080550 were not associated with the risk of total male infertility, NOA, or oligozoospermia. 30863997

2019