|
rs10861905
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer.
|
20932654 |
2010 |
|
rs10861905
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer.
|
20932654 |
2010 |
|
rs12336160
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer.
|
20932654 |
2010 |
|
rs12336160
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer.
|
20932654 |
2010 |
|
rs1527243
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer.
|
20932654 |
2010 |
|
rs1527243
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer.
|
20932654 |
2010 |
|
rs9810233
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Two single nucleotide polymorphisms located on chromosome 3 in 1 genomic loci were associated with erectile dysfunction with p <1 × 10(-6), including rs9810233 with p = 7 × 10(-7) and rs1920201 with p = 9 ×10(-7).
|
22704111 |
2012 |
|
rs9810233
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
Two single nucleotide polymorphisms located on chromosome 3 in 1 genomic loci were associated with erectile dysfunction with p <1 × 10(-6), including rs9810233 with p = 7 × 10(-7) and rs1920201 with p = 9 ×10(-7).
|
22704111 |
2012 |
|
rs17185536
|
|
T |
0.710 |
GeneticVariation |
GWASCAT |
In the discovery cohort, we identified a single locus (rs17185536-T) on chromosome 6 near the single-minded family basic helix-loop-helix transcription factor 1 (<i>SIM1</i>) gene that was significantly associated with the risk of erectile dysfunction (odds ratio = 1.26, <i>P</i> = 3.4 × 10<sup>-25</sup>).
|
30297428 |
2018 |
|
rs17185536
|
|
|
0.710 |
GeneticVariation |
BEFREE |
In the discovery cohort, we identified a single locus (rs17185536-T) on chromosome 6 near the single-minded family basic helix-loop-helix transcription factor 1 (<i>SIM1</i>) gene that was significantly associated with the risk of erectile dysfunction (odds ratio = 1.26, <i>P</i> = 3.4 × 10<sup>-25</sup>).
|
30297428 |
2018 |
|
rs57989773
|
|
|
0.710 |
GeneticVariation |
BEFREE |
We performed a genome-wide association study of ED in 6,175 case subjects among 223,805 European men and identified one locus at 6q16.3 (lead variant rs57989773, OR 1.20 per C-allele; p = 5.71 × 10<sup>-14</sup>), located between MCHR2 and SIM1.
|
30583798 |
2019 |
|
rs57989773
|
|
C |
0.710 |
GeneticVariation |
GWASCAT |
We performed a genome-wide association study of ED in 6,175 case subjects among 223,805 European men and identified one locus at 6q16.3 (lead variant rs57989773, OR 1.20 per C-allele; p = 5.71 × 10<sup>-14</sup>), located between MCHR2 and SIM1.
|
30583798 |
2019 |
|
rs305061
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.
|
22704111 |
2012 |
|
rs9378805
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.
|
22704111 |
2012 |
|
rs9850225
|
|
A |
0.700 |
GeneticVariation |
GWASDB |
Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.
|
22704111 |
2012 |
|
rs79721419
|
|
|
0.010 |
GeneticVariation |
BEFREE |
For POAG, an AD signal was observed at the 9p21 European descent (ED) POAG signal (rs79721419; P < 6.5×10<sup>-5</sup>) independent of the previously observed 9p21 ED signal (rs2383204; P < 2.3×10<sup>-5</sup>) by conditional analyses.
|
30352225 |
2019 |
|
rs1415088003
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The insertion/deletion (I/D) polymorphism in the angiotensin-converting enzyme gene (ACE) and the C825T polymorphism in the G-protein β3 subunit gene (GNB3) are associated with the efficacy of phosphodiesterase-5 inhibitor (PDE-5I) in erectile dysfunction.
|
26821322 |
2016 |
|
rs1415088003
|
|
|
0.020 |
GeneticVariation |
BEFREE |
In contrast to the previous studies in this analysis, the risk to develop ED is not influenced by the genotypes in the GNB3 C825T, the ACE I/D and the eNOS G894T polymorphisms.
|
20629643 |
2010 |
|
rs17483466
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.
|
22704111 |
2012 |
|
rs2781659
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ARG1 rs2781659 AA and rs2781667 TT genotypes are associated with lower IIEF scores (higher severity) only in clinical ED.
|
26537638 |
2015 |
|
rs2254298
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Importantly, the combination of having had anorexia and carrying either of the A alleles for two SNPS in the OXTR gene (rs53576, rs2254298) was associated with increased severity specifically for ED symptoms including cognitions and behaviors associated both with eating and appearance.
|
26106053 |
2015 |
|
rs53576
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Importantly, the combination of having had anorexia and carrying either of the A alleles for two SNPS in the OXTR gene (rs53576, rs2254298) was associated with increased severity specifically for ED symptoms including cognitions and behaviors associated both with eating and appearance.
|
26106053 |
2015 |
|
rs140186760
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology.
|
30583798 |
2019 |
|
rs2383204
|
|
|
0.010 |
GeneticVariation |
BEFREE |
For POAG, an AD signal was observed at the 9p21 European descent (ED) POAG signal (rs79721419; P < 6.5×10<sup>-5</sup>) independent of the previously observed 9p21 ED signal (rs2383204; P < 2.3×10<sup>-5</sup>) by conditional analyses.
|
30352225 |
2019 |
|
rs7176508
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.
|
22704111 |
2012 |