Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1366668789
rs1366668789
TBK1
CUI: C4225325
Disease: FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4 		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: rs1366668789
rs1366668789
TBK1
CUI: C4225325
Disease: FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4 		0.700 GeneticVariation UNIPROT Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia. 25803835

2015