PRUNE2, prune homolog 2 with BCH domain, 158471

N. diseases: 29; N. variants: 6
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 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. 19668339 2009
CUI: C4315130
Disease: Hippocampal atrophy
Hippocampal atrophy 		0.100 GeneticVariation phenotype GWASCAT Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. 19668339 2009