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SNP information rs610932

RS610932

Normal allele: GG

Polymorphism rs610932 is related to topics like this:

Alzheimer's disease is hereditary

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


Research and publications:

  19734902   Genome-wide association study identifies CLU and PICALM variants associated with Alzheimer's disease.

  21460840   Common variants ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.

  22047634   Alzheimer's Disease Neuroimaging Initiative: A review of articles published since its inception.

  22159054   A comprehensive genetic association study of Alzheimer disease in African Americans.

  22382309   Prevalence of CD33 and MS4A6A variant in a Chinese Han population with Alzheimer's disease.

  22833209   Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment.

  23180304   Genetic risk assessment predicting accelerated progression from mild cognitive impairment to Alzheimer's disease.

  23232270   Association of GWAS-associated loci with late-onset Alzheimer's disease in a Northern Han Chinese population.

  23573206   Genetic loci associated with Alzheimer's disease and cerebrospinal fluid biomarkers in a Finnish case-control cohort.

  24064185   Alzheimer's disease susceptibility variants in the MS4A6A gene are associated with altered levels of MS4A6A expression in the blood.

  24743338   Connecting the dots: the potential of data integration to identify regulatory SNPs in late-onset Alzheimer's disease GWAS results.

  24755620   Overrepresentation of glutamate signaling in Alzheimer's disease: enrichment of network pathways using meta-analysis of genome-wide association studies.

  25189118   Risk variants for late-onset Alzheimer's disease include memory loss, mild cognitive impairment, and Alzheimer's disease.

  25649863   Identifying genetic interactions associated with late-onset Alzheimer's disease.

  26455864   Association of CD33 and MS4A cluster variants with Alzheimer's disease in East Asian populations.

  26923404   Common variants in ABCA7 and MS4A6A are associated with cortical and hippocampal atrophy.

  27085534   The GBA, DYRK1A and MS4A6A polymorphisms influence the age at onset of Chinese Parkinson patients.

  27215977   miRNA-dependent target regulation: functional characterization of single nucleotide polymorphisms identified in genome-wide association studies of Alzheimer's disease.

  27274215   Genes associated with Alzheimer's disease: review and current status.

  27328823   Genome-wide identification of microRNA variants associated with Alzheimer's disease risk.

  27610127   Analysis of heterogeneous multimodal biomarkers of Alzheimer's disease using a Bayesian network.

  28477215   Validation of GWAS variants from microglial genes involved in Alzheimer's disease.

  28650998   Functional annotation of Alzheimer's disease-associated loci identified by GWAS.

  29504051   Updated meta-analysis of BIN1, CR1, MS4A6A, CLU, and ABCA7 variants in Alzheimer's disease.

  30378268   Association of genetic loci of Alzheimer's disease with mild behavioral disorders.

  33815092   Genetic variation in molecular pathways associated with Alzheimer's disease: a comprehensive review.

  34975449   Structural covariance network as an endophenotype in Alzheimer's disease susceptibility single nucleotide polymorphisms and correlations with cognitive outcomes.

  35537244   Generation of iPSC line KEIOi005-A from urine-derived cells (UDC) of a donor with mild Alzheimer's disease (AD) with multiple-risk SNPs for sporadic Alzheimer's disease (SAD).

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...

Genetics and atherosclerosis

Atherosclerosis is a progressive inflammatory disorder that underlies coronary artery disease (CAD)...

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