Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis (ALS) is a multifactorial condition, as both genetic and non-genetic factors are likely to play a role in the development of this diseases. Families in which there are multiple affected, close relatives are called familial and these cases are more likely to have a genetic cause.
Clinical genetic testing for familial ALS is complex as the condition can be caused by mutations in different genes.
This testing is for medical, clinical purposes.
This testing is only available through offline genetic testing providers if indicated by further evaluation and consultation with a trained genetic professional. Use the zip code search box to find a trained genetic professional in your area.
Amyotrophic Lateral Sclerosis (as part of Whole Genome Scan)
Informational genetic testing for susceptibility to ALS may be available as part of a whole genome scan.
Whole genome scanning looks for SNPs that are present throughout the entire genome that have been linked to susceptibility to a number of different health conditions and physical traits. A SNP is a genetic change in which one "letter" of DNA differs from the usual "letter" at that point in the DNA sequence. The number of conditions, traits, and SNPs tested for varies by provider.
Whole genome scanning is for informational purposes only and is not a medical (clinical) genetic test.
This testing is available online through the Direct-to-Consumer Genetic Testing providers listed below. A consultation with a trained genetic professional may be useful.
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