LASP1, LIM and SH3 protein 1, 3927

N. diseases: 85; N. variants: 3
Disease: Impaired cognition ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs140564516
rs140564516
Entrez Id: 3927
Gene Symbol: LASP1
LASP1
CUI: C0338656
Disease:
Impaired cognition 		A 0.700 GeneticVariation GWASCAT Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. 26252872 2015