Upload the DNA data file of the test

23andMe, AncestryDNA, FamilyTreeDNA, MyHeritage

and get an enhanced
personalized health report
free without registration

Files accepted .txt, .csv, .zip, .csv.gz

File data is not stored on the server

SNP information rs1858830

Normal allele: GG

Associated with a 2-fold increase in autism risk based on research. Responsible for impaired cortical MET signalling in autism spectrum disorders.

Polymorphism rs1858830 is related to topics like this:


Research and publications:

  17053076   A genetic variant that disrupts MET transcription is associated with autism.

  17696172   Disruption of cerebral cortex MET signaling in autism spectrum disorder.

  19002214   MET and autism susceptibility: family and case-control studies.

  19255034   Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions.

  19360663   Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.

  19548256   Association of MET with social and communication phenotypes in individuals with autism spectrum disorder.

  19681062   Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder.

  20080979   Association of genetic variation in the MET proto-oncogene with schizophrenia and general cognitive ability.

  20615438   Further evidence for the role of MET in autism susceptibility.

  22110649   Replication of the association of a MET variant with autism in a Chinese Han population.

  22558359   MET and AKT genetic influence on facial emotion perception.

  23715297   Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder.

  24150225   Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome.

  24240654   Autism spectrum disorder: interaction of air pollution with the MET receptor tyrosine kinase gene.

  24909855   A familial heterozygous null mutation of MET in autism spectrum disorder.

  24955105   Identification of SNP barcode biomarkers for genes associated with facial emotion perception using particle swarm optimization algorithm.

  26322220   A comprehensive meta-analysis of common genetic variants in autism spectrum conditions.

  29255778   Differential impact of Met receptor gene interaction with early-life stress on neuronal morphology and behavior in mice.

  34502168   Influence of the Aryl Hydrocarbon Receptor Activating Environmental Pollutants on Autism Spectrum Disorder.

  34929192   Evidence of susceptibility to autism risks associated with early life ambient air pollution: A systematic review.