Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1366668789
rs1366668789
TBK1
0.700 GeneticVariation UNIPROT Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia. 25803835

2015
dbSNP: rs1366668789
rs1366668789
TBK1
0.700 GeneticVariation UNIPROT Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease. 25943890

2015
dbSNP: rs1555204731
rs1555204731
TBK1
C 0.700 CausalMutation CLINVAR Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways. 25700176

2015
dbSNP: rs201970436
rs201970436
TBK1
0.700 GeneticVariation UNIPROT Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia. 25803835

2015
dbSNP: rs201970436
rs201970436
TBK1
0.700 GeneticVariation UNIPROT Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease. 25943890

2015
dbSNP: rs876657404
rs876657404
TBK1
G 0.700 CausalMutation CLINVAR Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia. 25803835

2015
dbSNP: rs1565814492
rs1565814492
TBK1
TA 0.700 CausalMutation CLINVAR

dbSNP: rs748112833
rs748112833
TBK1
A 0.700 CausalMutation CLINVAR

dbSNP: rs755950225
rs755950225
TBK1
G 0.700 CausalMutation CLINVAR

dbSNP: rs756751089
rs756751089
TBK1
G 0.700 CausalMutation CLINVAR

dbSNP: rs758357594
rs758357594
TBK1
0.700 GeneticVariation UNIPROT

dbSNP: rs765035140
rs765035140
TBK1
0.700 GeneticVariation UNIPROT

dbSNP: rs767898276
rs767898276
TBK1
A 0.700 CausalMutation CLINVAR

dbSNP: rs770942184
rs770942184
TBK1
0.700 GeneticVariation UNIPROT

dbSNP: rs876657405
rs876657405
TBK1
C 0.700 CausalMutation CLINVAR

dbSNP: rs876657406
rs876657406
TBK1
C 0.700 CausalMutation CLINVAR