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.