296
edits
Changes
→The PharmCAT method
*Only one PGx allele can exist simultaneously for the same patient
*But whenever we have additional variants, no PGx alleles will be reported
(Note that in practice also PharmCAT lets the PharmCAT software is agnostic about different user decide which allele definitions to use in their [https://github.com/PharmGKB/PharmCAT/wiki/NamedAlleleMatcher-101 NamedAlleleMatcher])
==Which definition should we stick to?==