Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5848
rs5848
GRN ; FAM171A2
0.040 GeneticVariation BEFREE The purpose of this meta-analysis was to investigate the association between progranulin polymorphism rs5848 and risk of the neurodegenerative diseases frontotemporal lobar degeneration (FTLD), Alzheimer's disease (AD), Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS). 25578179

2015
dbSNP: rs5848
rs5848
GRN ; FAM171A2
0.040 GeneticVariation BEFREE A single nucleotide polymorphism GRN rs5848 (3'UTR+78 C>T) was reported to alter the risk for frontotemporal lobar degeneration. 23342160

2013
dbSNP: rs5848
rs5848
GRN ; FAM171A2
0.040 GeneticVariation BEFREE We have attempted to rep</span>licate the association of rs5848</span> in three independent FTLD cohorts. 19446372

2011
dbSNP: rs5848
rs5848
GRN ; FAM171A2
0.040 GeneticVariation BEFREE The evidence presented here suggests that variation at rs5848 does not contribute to the etiology of FTLD in the Dutch population. 19847305

2009