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 the PharmCAT software may allow alleles to be defined in the SNP-array wayin their [https://github.com/PharmGKB/PharmCAT/wiki/NamedAlleleMatcher-101 NamedAlleleMatcher])
==Which definition should we stick to?==