rs10675541
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Progressive supranuclear palsy
0.700
GeneticVariation
GWASCAT
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases.
30089514
2018
rs1707957
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Non-obstructive azoospermia
0.700
GeneticVariation
GWASDB
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
22197933
2011
rs1768208
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Progressive supranuclear palsy
0.830
GeneticVariation
GWASDB
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
21685912
2011
rs1768208
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Progressive supranuclear palsy
0.830
GeneticVariation
BEFREE
Testing for association of CBD with top progressive supranuclear palsy (PSP ) GWAS single-nucleotide polymorphisms (SNPs) identified associations at MOBP (3p22; rs1768208 ; P=2.07 × 10(-7)) and MAPT H1c (17q21; rs242557; P=7.91 × 10(-6)).
26077951
2015
rs1768208
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Progressive supranuclear palsy
0.830
GeneticVariation
BEFREE
Meta-analysis revealed highly significant associations for PSP risk alleles of rs8070723 and rs1768208 with higher LRRC37A4 and MOBP brain levels, respectively.
27115769
2016
rs1768208
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Progressive supranuclear palsy
0.830
GeneticVariation
GWASCAT
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
21685912
2011
rs1768208
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Progressive supranuclear palsy
0.830
GeneticVariation
BEFREE
An SNP (rs1768208 C/T) has been identified as a strong risk factor for PSP .
26335643
2015
rs1768208
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Corticobasal degeneration
0.700
GeneticVariation
GWASCAT
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.
26077951
2015
rs1768208
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Deuteranomaly
0.010
GeneticVariation
BEFREE
Testing for association of CBD with top progressive supranuclear palsy (PSP) GWAS single-nucleotide polymorphisms (SNPs) identified associations at MOBP (3p22; rs1768208 ; P=2.07 × 10(-7)) and MAPT H1c (17q21; rs242557; P=7.91 × 10(-6)).
26077951
2015
rs1768208
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Behavioral variant of frontotemporal dementia
0.010
GeneticVariation
BEFREE
The rs1768208 risk polymorphism in MOBP may have prognostic value in bvFTD .
24994843
2014
rs1768244
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Diarrhoea predominant irritable bowel syndrome
0.010
GeneticVariation
BEFREE
Interaction tests of KLB rs17618244 with 3 nonsynonymous SNPs of fibroblast growth factor receptor 4 (FGFR4) revealed that rs1966265 (Val10Ile) and rs351855 (Gly388Arg) modulate rs1768244 's association with colonic transit in IBS-D (P=.0025 and P=.0023, respectively).
21396369
2011
rs538867
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Alzheimer's Disease
0.800
GeneticVariation
GWASDB
Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
23535033
2014
rs538867
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Alzheimer's Disease
0.800
GeneticVariation
GWASCAT
Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
23535033
2014
rs616147
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
0.700
GeneticVariation
GWASCAT
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
28931804
2017
rs616147
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Amyotrophic Lateral Sclerosis
0.700
GeneticVariation
GWASCAT
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.
27455348
2016
rs616147
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.700
GeneticVariation
GWASCAT
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
28931804
2017
rs616147
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
AMYOTROPHIC LATERAL SCLEROSIS 1
0.700
GeneticVariation
GWASCAT
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
28931804
2017
rs616147
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Amyotrophic Lateral Sclerosis, Sporadic
0.700
GeneticVariation
GWASCAT
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
28931804
2017
rs864643
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Attention deficit hyperactivity disorder
0.800
GeneticVariation
GWASDB
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.
18839057
2008
rs864643
×
Entrez Id:
4336
Gene Symbol:
MOBP
MOBP
Attention deficit hyperactivity disorder
0.800
GeneticVariation
GWASCAT
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.
18839057
2008