VPS13B, vacuolar protein sorting 13 homolog B, 157680

N. diseases: 158; N. variants: 309
Disease: Hippocampal atrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4315130
Disease: Hippocampal atrophy
Hippocampal atrophy 		0.100 GeneticVariation phenotype GWASDB Multiple loci influencing hippocampal degeneration identified by genome scan. 22745009 2012
CUI: C4315130
Disease: Hippocampal atrophy
Hippocampal atrophy 		0.100 GeneticVariation phenotype GWASCAT Multiple loci influencing hippocampal degeneration identified by genome scan. 22745009 2012