296
edits
Changes
m
→How to define PGx alleles
==How to define PGx alleles==
PGx alleles are defined as collections of one or more SNPs, INDELs or structural variants. When a patient is sequenced by next generation sequencing ([[NGS]]) we may typically observe more variants than those which are included in any individual PGx allele definitions.
[[File:Variant tree outline.png|thumb|The 16 possible haplotypes for a four loci, decomposed variant calling]]
This means that
