Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10248566
rs10248566
0.700 GeneticVariation GWASDB A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. 22197933

2011

dbSNP: rs1039229
rs1039229
0.700 GeneticVariation GWASDB A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. 22197933

2011

dbSNP: rs10842262
rs10842262
0.720 GeneticVariation GWASDB The combined analyses identified significant (P < 5.0 × 10(-8)) associations between NOA risk and common variants near PRMT6 (rs12097821 at 1p13.3: odds ratio (OR) = 1.25, P = 5.7 × 10(-10)), PEX10 (rs2477686 at 1p36.32: OR = 1.39, P = 5.7 × 10(-12)) and SOX5 (rs10842262 at 12p12.1: OR = 1.23, P = 2.3 × 10(-9)). 22197933

2011

dbSNP: rs10842262
rs10842262
0.720 GeneticVariation BEFREE Interestingly, the normozoospermic males with the risk genotypes of rs12097821 and rs3129878 + rs10842262 + rs12097821 were observed to have higher total sperm counts relative to non-risk genotypes, suggesting that the risk alleles of the genetic loci may not be via impairing spermatogenic ability to express susceptibility to NOA. 25505198

2015

dbSNP: rs10842262
rs10842262
0.720 GeneticVariation BEFREE The combined analyses identified significant (P < 5.0 × 10(-8)) associations between NOA risk and common variants near PRMT6 (rs12097821 at 1p13.3: odds ratio (OR) = 1.25, P = 5.7 × 10(-10)), PEX10 (rs2477686 at 1p36.32: OR = 1.39, P = 5.7 × 10(-12)) and SOX5 (rs10842262 at 12p12.1: OR = 1.23, P = 2.3 × 10(-9)). 22197933

2011

dbSNP: rs10910078
rs10910078
0.700 GeneticVariation GWASDB A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. 22197933

2011

dbSNP: rs10978121
rs10978121
0.700 GeneticVariation GWASDB A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. 22197933

2011

dbSNP: rs11135484
rs11135484
0.010 GeneticVariation BEFREE Our results demonstrated that there was a suggestively significant interaction between Y-hg O3e(*) and rs11135484 on NOA (Pinter = 9.89 × 10(-5)). 27628680

2016

dbSNP: rs11204885
rs11204885
0.700 GeneticVariation GWASDB A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. 22197933

2011

dbSNP: rs11754464
rs11754464
0.010 GeneticVariation BEFREE We identified three low-frequency variants located at 6p22.2 (rs2298090 in HIST1H1E encoding p.Lys152Arg: OR = 0.30, P = 2.40 × 10(-16)) and 6p21.33 (rs200847762 in FKBPL encoding p.Pro137Leu: OR = 0.11, P = 3.77 × 10(-16); rs11754464 in MSH5: OR = 1.78, P = 3.71 × 10(-7)) associated with NOA risk after Bonferroni correction. 26199320

2015

dbSNP: rs11918142
rs11918142
0.700 GeneticVariation GWASDB A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. 22197933

2011

dbSNP: rs11937871
rs11937871
0.700 GeneticVariation GWASDB A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. 22197933

2011

dbSNP: rs11987150
rs11987150
0.700 GeneticVariation GWASDB A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. 22197933

2011

dbSNP: rs12097821
rs12097821
0.720 GeneticVariation GWASDB The combined analyses identified significant (P < 5.0 × 10(-8)) associations between NOA risk and common variants near PRMT6 (rs12097821 at 1p13.3: odds ratio (OR) = 1.25, P = 5.7 × 10(-10)), PEX10 (rs2477686 at 1p36.32: OR = 1.39, P = 5.7 × 10(-12)) and SOX5 (rs10842262 at 12p12.1: OR = 1.23, P = 2.3 × 10(-9)). 22197933

2011

dbSNP: rs12097821
rs12097821
0.720 GeneticVariation BEFREE Interestingly, the normozoospermic males with the risk genotypes of rs12097821 and rs3129878 + rs10842262 + rs12097821 were observed to have higher total sperm counts relative to non-risk genotypes, suggesting that the risk alleles of the genetic loci may not be via impairing spermatogenic ability to express susceptibility to NOA. 25505198

2015

dbSNP: rs12097821
rs12097821
0.720 GeneticVariation BEFREE The combined analyses identified significant (P < 5.0 × 10(-8)) associations between NOA risk and common variants near PRMT6 (rs12097821 at 1p13.3: odds ratio (OR) = 1.25, P = 5.7 × 10(-10)), PEX10 (rs2477686 at 1p36.32: OR = 1.39, P = 5.7 × 10(-12)) and SOX5 (rs10842262 at 12p12.1: OR = 1.23, P = 2.3 × 10(-9)). 22197933

2011

dbSNP: rs121908940
rs121908940
A 0.700 GeneticVariation CLINVAR

dbSNP: rs12429186
rs12429186
0.700 GeneticVariation GWASDB A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. 22197933

2011

dbSNP: rs12614
rs12614
0.700 GeneticVariation GWASDB A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia. 22541561

2012

dbSNP: rs13206743
rs13206743
0.010 GeneticVariation BEFREE We find strong evidence of three NOA susceptibility loci (P<5.0 × 10(-8)) at 6p21.32 (rs7194, P=3.76 × 10(-19)), 10q25.3 (rs7099208, P=6.41 × 10(-14)) and 6p12.2 (rs13206743, P=3.69 × 10(-8)), as well as one locus approaching genome-wide significance at 1q42.13 (rs3000811, P=7.26 × 10(-8)). 24852083

2014

dbSNP: rs1328626
rs1328626
0.010 GeneticVariation BEFREE The polymorphisms rs1328626 and rs6563386 of the SOHLH2 gene would be the genetic risk factors for NOA in the Chinese population. 25463635

2015

dbSNP: rs1328641
rs1328641
0.010 GeneticVariation BEFREE The SNP rs1328641 might influence testes development in the NOA patients. 25463635

2015

dbSNP: rs138178131
rs138178131
0.010 GeneticVariation BEFREE PGAM4 coding region mutations were not observed and the G75C polymorphism is not associated with NOA susceptibility among the Chinese Han population. 23631659

2013

dbSNP: rs140506267
rs140506267
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1406714
rs1406714
0.010 GeneticVariation BEFREE Combined analysis using directly genotyped data for Stages 1 and 2 revealed that rs1406714 in CHD2 was associated with decreased risk of NOA [odds ratio (OR) = 0.78, 95% confidence interval (CI) = 0.68-0.89, Pmeta = 1.7E-04], whereas rs2126986 in GNAO1 and rs7226979 in BCL2 were both risk makers for NOA (rs2126986: OR = 1.28, 95% CI = 1.15-1.41, Pmeta = 2.3E-06; rs7226979: OR = 1.21, 95% CI = 1.11-1.33, Pmeta = 4.5E-05). 24549219

2014