Rare diseases

This module analyses the 'inherited conditions' module from 23andme from 2016. These conditions were all rare, but strong genetic effects. Additionally the module tries to translate the data for non-23andme customers, with the caveat that because the SNPs are very rare they are often hard to impute.

To run analysis input your user-id, or use the test-value of id_613z86871:

The table shows the variants which are known to confer a range of severe inherited conditions. They are all fairly rare conditions. Slightly more common, however, is the case of being a carrier of these conditions. Being a carrier means that a person have one copy of a disease-causing allele, but will not be affected because the condition only manifests if both copies are of the disease-causing type.