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SNP information rs8070723

RS8070723

Normal allele: AA

Polymorphism rs8070723 is related to topics like this:

Parkinson is a genetic disease

A disorder that progresses gradually within the nervous system is known as Parkinson's disease. It...

Dementia is genetic

Dementia is characterized as a syndrome, rather than a singular disease. Individuals with early...

Alzheimer's disease is hereditary

Alzheimer's disease is a degenerative brain disease that causes dementia, resulting in a gradual...


Research and publications:

  18985386   Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

  20070850   Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.

  21248740   Genome-wide association study confirms extant PD risk loci among the Dutch.

  21685912   Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.

  21833654   Biomarkers to identify the pathological basis for frontotemporal lobar degeneration.

  24373676   Genetic and neuroanatomic associations in sporadic frontotemporal lobar degeneration.

  24994843   Myelin oligodendrocyte basic protein and prognosis in behavioral-variant frontotemporal dementia.

  25778476   A novel Alzheimer disease locus located near the gene encoding tau protein.

  26077951   Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.

  26154020   A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia.

  27115769   Gene expression, methylation and neuropathology correlations at progressive supranuclear palsy risk loci.

  27900365   Genome sequencing in a case of Niemann-Pick type C.

  28189700   CSF protein changes associated with hippocampal sclerosis risk gene variants highlight impact of GRN/PGRN.

  30154825   To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes.

  31234228   Association of MAPT H1 subhaplotypes with neuropathology of lewy body disease.

  32400971   MAPT haplotype-stratified GWAS reveals differential association for AD risk variants.

  33635380   Latent trait modeling of tau neuropathology in progressive supranuclear palsy.

Is multiple sclerosis hereditary disease

The presence of lesions on the brain and spinal cord is indicative of multiple sclerosis, a...

Is OCD obsessive compulsive disorder genetic

Obsessive-compulsive disorder (OCD) is a mental health condition characterized by features known as...

Suicide genetic

Suicide is a serious public health crisis and it has been getting progressively worse. In the past...

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