Next Generation Sequencing | Deletion / Duplication | NGS & Del Dup Comprehensive |
---|---|---|
Price: $950
|
Price: $750
|
Price: $1600
|
CPT: 81406
|
CPT: 81405
|
CPT: 81406
81405
|
Variants in PYGM are associated with autosomal recessive Glycogen Storage Disease type V, also known as McArdle disease. This test will detect the two most common variants, p.Arg50Ter and p.Gly205Ser as well as any other sequencing error. Large deletions of PYGM are rare and will not be detected by NGS.
Type E
4 weeks or less