Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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