Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750306
rs63750306
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
0.050 GeneticVariation BEFREE Here, we report that the expression of FAD-linked PS1 M146V mutant affects store-operated calcium channel activity (Isoc) in human neuroblastoma SK-N-SH cells. 23624206

2013

dbSNP: rs63750306
rs63750306
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
0.050 GeneticVariation BEFREE To elucidate the role of presenilin-1 in the Alzheimer's disease pathology, we tested two such mutations (P117L and M146L) for their effect in stably transfected mouse neuroblastoma cell lines. 11311782

2001

dbSNP: rs63750306
rs63750306
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
0.050 GeneticVariation BEFREE Two (P117L; M146L) familial Alzheimer's disease (FAD)-causing presenilin-1 (PS1) mutations have been tested fortheir effect in stably transfected mouse neuroblastoma (N2a) cell lines. 10400232

1999

dbSNP: rs63750306
rs63750306
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
0.050 GeneticVariation BEFREE To investigate the pathogenic mechanism of PS1 mutations linked to FAD, we established inducible mouse neuroblastoma (Neuro 2a) cell lines expressing the human wild-type (wt) or mutated PS1(M146L or deltaexon 10) under the control of the Lac repressor. 10360683

1999

dbSNP: rs63750306
rs63750306
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
0.050 GeneticVariation BEFREE The influence of PS1 mutations on the generation of endogenous intracellular amyloid beta-protein (A beta) species was assessed using a highly sensitive immunoblotting technique with inducible mouse neuroblastoma (Neuro 2a) cell lines expressing the human wild-type (wt) or mutated PS1 (M146L or delta exon 10). 9751187

1998