SCNN1G - autosomal recessive pseudohypoaldosteronism

This test is available for the following conditions:

  • Conditions > Endocrine > Pseudohypoaldosteronism type 1
  • Conditions > Renal / Nephrological > Pseudohypoaldosteronism type 1

This product is also part of the following panels:

  • WES comprehensive preconception carrier test *
  • WES Mendelian inherited disorders (97.2% **)
  • WES renal disorders (97.2% **)

** % 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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 600761
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 402

Gene

NR3C2 - autosomal dominant pseudohypoaldosteronism type 1

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 393

NR3C2 - autosomal dominant pseudohypoaldosteronism type 1



€ 393

NR3C2 - autosomal dominant pseudohypoaldosteronism type 1

This test is available for the following conditions:

  • Conditions > Endocrine > Pseudohypoaldosteronism type 1
  • Conditions > Renal / Nephrological > Pseudohypoaldosteronism type 1

This product is also part of the following panels:

  • WES Mendelian inherited disorders (98.1% **)
  • WES renal disorders (98.1% **)

** % 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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 600983
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 393
Gene

SCNN1A - autosomal recessive pseudohypoaldosteronism

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 385

SCNN1A - autosomal recessive pseudohypoaldosteronism



€ 385

SCNN1A - autosomal recessive pseudohypoaldosteronism

This test is available for the following conditions:

  • Conditions > Endocrine > Pseudohypoaldosteronism type 1
  • Conditions > Renal / Nephrological > Pseudohypoaldosteronism type 1

This product is also part of the following panels:

  • WES comprehensive preconception carrier test *
  • WES Mendelian inherited disorders (98.3% **)
  • WES renal disorders (98.3% **)

** % 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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 600228
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 385
Gene

SCNN1B - autosomal recessive pseudohypoaldosteronism

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 410

SCNN1B - autosomal recessive pseudohypoaldosteronism



€ 410

SCNN1B - autosomal recessive pseudohypoaldosteronism

This test is available for the following conditions:

  • Conditions > Endocrine > Pseudohypoaldosteronism type 1
  • Conditions > Renal / Nephrological > Pseudohypoaldosteronism type 1

This product is also part of the following panels:

  • WES comprehensive preconception carrier test *
  • WES Mendelian inherited disorders (100.0% **)
  • WES renal disorders (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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 600760
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 410
Gene

SCNN1G - autosomal recessive pseudohypoaldosteronism

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 402

SCNN1G - autosomal recessive pseudohypoaldosteronism



€ 402