Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs864643
rs864643
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C1263846
Disease:
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
dbSNP: rs864643
rs864643
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C1263846
Disease:
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
dbSNP: rs1768208
rs1768208
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C0038868
Disease:
Progressive supranuclear palsy
0.830 GeneticVariation GWASCAT Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. 21685912 2011
dbSNP: rs1768208
rs1768208
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C0038868
Disease:
Progressive supranuclear palsy
0.830 GeneticVariation GWASDB Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. 21685912 2011
dbSNP: rs1707957
rs1707957
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C4021107
Disease:
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
dbSNP: rs1768244
rs1768244
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C1262211
Disease:
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
dbSNP: rs538867
rs538867
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C0002395
Disease:
Alzheimer's Disease
0.800 GeneticVariation GWASCAT Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. 23535033 2014
dbSNP: rs538867
rs538867
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C0002395
Disease:
Alzheimer's Disease
0.800 GeneticVariation GWASDB Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. 23535033 2014
dbSNP: rs1768208
rs1768208
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C4011788
Disease:
Behavioral variant of frontotemporal dementia
0.010 GeneticVariation BEFREE The rs1768208 risk polymorphism in MOBP may have prognostic value in bvFTD. 24994843 2014
dbSNP: rs1768208
rs1768208
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C0038868
Disease:
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
dbSNP: rs1768208
rs1768208
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C0038868
Disease:
Progressive supranuclear palsy
0.830 GeneticVariation BEFREE An SNP (rs1768208 C/T) has been identified as a strong risk factor for PSP. 26335643 2015
dbSNP: rs1768208
rs1768208
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C0393570
Disease:
Corticobasal degeneration
0.700 GeneticVariation GWASCAT Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. 26077951 2015
dbSNP: rs1768208
rs1768208
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C3887938
Disease:
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
dbSNP: rs1768208
rs1768208
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C0038868
Disease:
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
dbSNP: rs616147
rs616147
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C0002736
Disease:
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
dbSNP: rs616147
rs616147
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C1842675
Disease:
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
dbSNP: rs616147
rs616147
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C1862939
Disease:
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
dbSNP: rs616147
rs616147
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C1862941
Disease:
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
dbSNP: rs616147
rs616147
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C3542025
Disease:
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
dbSNP: rs10675541
rs10675541
Entrez Id: 4336
Gene Symbol: MOBP
MOBP
CUI: C0038868
Disease:
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