ScopeKlinikum der Universität Augsburg (Universitätsklinikum Augsburg) Institut für Humangenetik
29 capabilities
Accredited since May 2026
Verified May 2026
One of 3,188 in Germany
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Details
Stenglinstraße 2
Augsburg 86156 , Germany
Augsburg 86156 , Germany
Accreditation
Active
DAkkS
D-ML-13136-01-01
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-13136-01-01
Status
ActiveSince
04 May 2026
Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.
Download Scope PDFAdditional scope documents
Test Capabilities (29)
| Standard Reference | Description | Category |
|---|---|---|
| (DICER1 ); SNV, CNV | (DICER1 ); SNV, CNV | Molecular Diagnostics / PCR |
| (PDGFRB, NOTCH3 ); SNV, CNV | (PDGFRB, NOTCH3 ); SNV, CNV | Molecular Diagnostics / PCR |
| 1/4 (DKN1B, MEN1 ); SNV, CNV | 1/4 (DKN1B, MEN1 ); SNV, CNV | Molecular Diagnostics / PCR |
| Brust- und Eierstockkrebs | Familiärer Brust- und Eierstockkrebs | Molecular Diagnostics / PCR |
| DICER1-assozierte Tumordisposition | DICER1-assozierte Tumordisposition | Molecular Diagnostics / PCR |
| Darmkrebs, adenomatöse Polyposis | Darmkrebs, adenomatöse Polyposis | Molecular Diagnostics / PCR |
| Endometriumkarzinom (FH, MLH1, MSH2, MSH6, PMS2, PTEN, EPCAM, MUTYH, NTHL1, POLD1, POLE, SMAD4 ); SNV, CNV | Endometriumkarzinom (FH, MLH1, MSH2, MSH6, PMS2, PTEN, EPCAM, MUTYH, NTHL1, POLD1, POLE, SMAD4 ); SNV, CNV | Molecular Diagnostics / PCR |
| Infantile Myofibromatose | Infantile Myofibromatose | Molecular Diagnostics / PCR |
| MSH2, MSH6, MUTYH, PMS2, PTEN, RAD51C, RAD51D, STK11, TP53 | MSH2, MSH6, MUTYH, PMS2, PTEN, RAD51C, RAD51D, STK11, TP53 | Molecular Diagnostics / PCR |
| Multiple Endokrine Neoplasie Typ | Multiple endokrine Neoplasie Typ | Molecular Diagnostics / PCR |
| Paragangliom, Phäochromozytom | Paragangliom, Phäochromozytom | Molecular Diagnostics / PCR |
| Rhythmusstörungen (ABCC9, AKAP9, ANK2,TTN); SNV, CNV | Rhythmusstörungen (ABCC9, AKAP9, ANK2,TTN); SNV, CNV | Molecular Diagnostics / PCR |
| Syndrom (PTEN ); SNV, CNV | Syndrom (PTEN ); SNV, CNV | Molecular Diagnostics / PCR |
| (TruSight Oncology 500 v2) (RET | (TruSight Oncology 500 v2) (RET | Other |
| 8,17,29,50,63), SAR1B, SCARB1, SMPD1, SORT1, SPRTN, USF1, WRN, ZMPSTE24; CNV: LDLR, LPL) | 8,17,29,50,63), SAR1B, SCARB1, SMPD1, SORT1, SPRTN, USF1, WRN, ZMPSTE24; CNV: LDLR, LPL) | Other |
| ATM, BRCA1,…,TP53); SNV, CNV | ATM, BRCA1,…,TP53); SNV, CNV | Other |
| Birt-Hogg-Dubé-Syndrom (FLCN | Birt-Hogg-Dubé-Syndrom (FLCN | Other |
| Foundervariante); SNV, CNV | Foundervariante); SNV, CNV | Other |
| MSH2, MSH6, EPCAM ); SNV, CNV | MSH2, MSH6, EPCAM ); SNV, CNV | Other |
| Noonan-Syndrom Basis (PTPN11 | Noonan-Syndrom Basis (PTPN11 | Other |
| POLE ); SNV, CNV | POLE ); SNV, CNV | Other |
| PTCH1 ); SNV, CNV | PTCH1 ); SNV, CNV | Other |
| Pankreaskarzinom, familiäres (APC | Pankreaskarzinom, familiäres (APC | Other |
| Peutz-Jeghers-Syndrom (STK11 | Peutz-Jeghers-Syndrom (STK11 | Other |
| RAD51D, HOXB13- | RAD51D, HOXB13- | Other |
| SMARCB1 ); SNV, CNV | SMARCB1 ); SNV, CNV | Other |
| Tuberöse Sklerose (TSC1, TSC2 | Tuberöse Sklerose (TSC1, TSC2 | Other |
| VHL, BAP1, TSC1, TSC2 ); SNV, CNV | VHL, BAP1, TSC1, TSC2 ); SNV, CNV | Other |
| bearbeitet und analysiert. | bearbeitet und analysiert. | Other |
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