rs76980269, NOS1

N. diseases: 10
Disease: Frontotemporal Lobar Degeneration ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Frontotemporal Lobar Degeneration
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
0.020 GeneticVariation BEFREE Neuronal nitric oxide synthase (NOS)1 C276T polymorphism was shown to increase the risk for frontotemporal lobar degeneration (FTLD). 19087148 2009
Frontotemporal Lobar Degeneration
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
0.020 GeneticVariation BEFREE The C276T SNP acts as risk factor for sporadic FTLD, possibly influencing NOS1 transcription. 18042235 2008