NCS1, neuronal calcium sensor 1, 23413

N. diseases: 48; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4836694
rs4836694
Entrez Id: 23413
Gene Symbol: NCS1
NCS1
CUI: C0002395
Disease:
Alzheimer's Disease 		0.800 GeneticVariation GWASDB Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. 23535033 2014
dbSNP: rs4836694
rs4836694
Entrez Id: 23413
Gene Symbol: NCS1
NCS1
CUI: C0002395
Disease:
Alzheimer's Disease 		0.800 GeneticVariation GWASCAT Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. 23535033 2014
dbSNP: rs370911031
rs370911031
Entrez Id: 23413
Gene Symbol: NCS1
NCS1
CUI: C1510586
Disease:
Autism Spectrum Disorders 		0.010 GeneticVariation BEFREE Mutations in IL1RAPL1 have recently been associated with autism spectrum disorders and a missense mutation (R102Q) on NCS-1 has been found in one individual with autism. 20479890 2010
dbSNP: rs370911031
rs370911031
Entrez Id: 23413
Gene Symbol: NCS1
NCS1
CUI: C0004352
Disease:
Autistic Disorder 		0.010 GeneticVariation BEFREE Mutations in IL1RAPL1 have recently been associated with autism spectrum disorders and a missense mutation (R102Q) on NCS-1 has been found in one individual with autism. 20479890 2010