STK11 - Peutz-Jeghers syndrome
This test is available for the following conditions:
- Conditions > Oncogenetics > Peutz-Jeghers syndrome
This product is also part of the following panels:
- panel polyposis (APC, MUTYH, SMAD4, BMPR1A, POLE, POLD1, NTHL1, STK11, PTEN)
- WES hereditary cancer (100.0% *)
- WES Mendelian inherited disorders (100.0% *)
- WES skin disorders¹ (100.0% *)
* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)
Turnaround time
Complete analysis & Targeted analysis: 3 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
- Deletion/duplication analysis (MLPA)
OMIM:
602216
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA