Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750707
rs63750707
GRN
A 0.700 GeneticVariation CLINVAR Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage. 22608501

2012
dbSNP: rs63750707
rs63750707
GRN
A 0.700 GeneticVariation CLINVAR Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. 16862116

2006
dbSNP: rs63750707
rs63750707
GRN
A 0.700 GeneticVariation CLINVAR Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. 16950801

2006