Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63751273
rs63751273
MAPT
0.010 GeneticVariation BEFREE We diagnosed all cases as pure SD and identified a P301L mutation in the MAPT gene of the proband. 21555888

2011
dbSNP: rs10814083
rs10814083
KIF24
0.010 GeneticVariation BEFREE The distribution of five Single Nucleotide Polymorphisms (SNPs) located in the chromosome 9 haplotype identified via linkage analysis, including UBAP1 rs7018487, UBAP2 rs1785506 and rs307658, and KIF24 rs17350674 and rs10814083, has been determined in a population of 284 patients diagnosed with FTLD, including 245 with behavioural variant Frontotemporal Dementia (bvFTD), 23 with Progressive Aphasia and 16 with Semantic Dementia, compared with 318 age-matched controls. 20670673

2010
dbSNP: rs63750869
rs63750869
MAPT
0.010 GeneticVariation BEFREE Semantic dementia associated with mutation V363I in the tau gene. 20598713

2010
dbSNP: rs201148958
rs201148958
IFT74
0.010 GeneticVariation BEFREE An additional sequence variant (G58D) was found in a case of sporadic semantic dementia. 17166276

2006