×
Entrez Id:
5789
Gene Symbol:
PTPRD
PTPRD
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
22197933
2011
HLA-DRB9
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia.
22541561
2012
TSBP1-AS1
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia.
22541561
2012
×
Entrez Id:
10665
Gene Symbol:
TSBP1
TSBP1
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia.
22541561
2012
×
Entrez Id:
1789
Gene Symbol:
DNMT3B
DNMT3B
0.100
GeneticVariation
disease
CLINVAR
NPAS2-AS1
0.100
GeneticVariation
disease
CLINVAR
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
22197933
2011
×
Entrez Id:
79695
Gene Symbol:
GALNT12
GALNT12
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
22197933
2011
LINC02150
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
22197933
2011
×
Entrez Id:
2195
Gene Symbol:
FAT1
FAT1
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
22197933
2011
×
Entrez Id:
5747
Gene Symbol:
PTK2
PTK2
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
22197933
2011
×
Entrez Id:
56244
Gene Symbol:
BTNL2
BTNL2
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia.
22541561
2012
×
Entrez Id:
728215
Gene Symbol:
FAM155A
FAM155A
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
22197933
2011
LINC02269
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
22197933
2011
×
Entrez Id:
8685
Gene Symbol:
MARCO
MARCO
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia.
22541561
2012
×
Entrez Id:
22856
Gene Symbol:
CHSY1
CHSY1
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
22197933
2011
×
Entrez Id:
9651
Gene Symbol:
PLCH2
PLCH2
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
22197933
2011
LINC01829
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia.
22541561
2012
×
Entrez Id:
4862
Gene Symbol:
NPAS2
NPAS2
0.100
GeneticVariation
disease
CLINVAR
×
Entrez Id:
560
Gene Symbol:
AZF1
AZF1
0.040
GeneticVariation
disease
BEFREE
Our results suggest that AZFa gene deletion is infrequent in Taiwanese patients with severe oligozoospermia or non-obstructive azoospermia .
11695273
2001
×
Entrez Id:
560
Gene Symbol:
AZF1
AZF1
0.040
GeneticVariation
disease
BEFREE
Aproximately 10% of patients with non-obstructive azoospermia and 5% with non-obstructive severe oligozoospermia carry AZF region microdeletions (AZoospermic Factor) in the Y chromosome.
24954841
2014
×
Entrez Id:
4524
Gene Symbol:
MTHFR
MTHFR
0.030
GeneticVariation
disease
BEFREE
The MTHFR 677TT genotype may be a genetic risk factor for male infertility, especially with severe OAT and non-obstructive azoospermia in unexplained infertile males.
16247718
2005
×
Entrez Id:
4524
Gene Symbol:
MTHFR
MTHFR
0.030
GeneticVariation
disease
BEFREE
DNA from peripheral blood (PB) samples of 50 patients with NOA and 50 fertile men (controls) as well as DNA from testicular biopsies of 32 patients with NOA and five patients with obstructive azoospemia, but normal spermatogenesis, were analyzed by Methylation Specific PCR amplification using primers that hybridize to the CpG island in the promoter region of MTHFR .
19477879
2009
×
Entrez Id:
4524
Gene Symbol:
MTHFR
MTHFR
0.030
GeneticVariation
disease
BEFREE
Our findings suggest the MTHFR c.1298A > C polymorphism is associated with an increased risk of male infertility, i.e., NOA .
26196053
2015
×
Entrez Id:
10734
Gene Symbol:
STAG3
STAG3
0.020
GeneticVariation
disease
BEFREE
The full coding region of STAG3 was sequenced directly in a cohort of 28 men with NOA due to meiotic arrest.
31682730
2019