SMARCB1 - Rhabdoid tumor predisposition syndrome type 1

This test is available for the following conditions:

  • Conditions > Oncogenetics > Rhabdoid tumor predisposition syndrome

This product is also part of the following panels:

  • WES hereditary cancer (% *)
  • WES intellectual disability (% *)
  • WES Mendelian inherited disorders (% *)
  • WES neurological pain disorders¹ (% *)
  • WES short stature/skeletal dysplasia (% *)
  • WES skin disorders¹ (% *)
  • WES sonic hedgehog medulloblastoma (% *)

* % 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
3 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 601607
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA, Buccal mucous membrane




€ 385

Gene

SMARCB1 - Rhabdoid tumor predisposition syndrome type 1

Turnaround time
3 weeks
Performing laboratory
Radboudumc
€ 385

SMARCB1 - Rhabdoid tumor predisposition syndrome type 1



€ 385