Klinikum der Universität Augsburg (Universitätsklinikum Augsburg) Institut für Humangenetik

42 capabilities Accredited since May 2026 Verified Oct 2026 One of 3,209 in Germany
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Details

Stenglinstraße 2
Augsburg 86156 , Germany

Accreditation

Active DAkkS D-ML-13136-01-01
www.uk-augsburg.de/einrichtungen/institute/inst... Prefer to enquire through us? Send an enquiry
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Performs molecular genetic diagnostic testing in human genetics, including analysis of hereditary conditions such as familial breast and ovarian cancer genes, using DNA extracted from blood and tissue samples.

Accreditation Details

Accreditation Body

DAkkS

Number

D-ML-13136-01-01

Status

Active

Since

04 May 2026

Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.

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Additional scope documents

Download Scope PDF · D-ML-13136-01-00

Test Capabilities (42)
Standard Reference Description Category
(APC, MUTYH, MSH3, POLD1, POLE ); SNV, CNV (APC, MUTYH, MSH3, POLD1, POLE ); SNV, CNV Molecular Diagnostics / PCR
(DICER1 ); SNV, CNV (DICER1 ); SNV, CNV Molecular Diagnostics / PCR
(MAX, RET, SDHAF2, SDHA, SDHB, SDHC, SDHD, TMEM127, VHL ); SNV, CNV (MAX, RET, SDHAF2, SDHA, SDHB, SDHC, SDHD, TMEM127, VHL ); 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
Birt-Hogg-Dubé-Syndrom (FLCN ); Birt-Hogg-Dubé-Syndrom (FLCN) Molecular Diagnostics / PCR
Brust- und Eierstockkrebs Familiärer Brust- und Eierstockkrebs Molecular Diagnostics / PCR
Carney Komplex (PRKAR1A); SNV, CNV Carney Komplex (PRKAR1A); SNV, CNV Molecular Diagnostics / PCR
Cowden-Syndrom /PTEN- assoziiertes Hamartom-Tumor- Syndrom (PTEN ); SNV, CNV Cowden-Syndrom /PTEN- assoziiertes Hamartom-Tumor- Syndrom (PTEN ); SNV, CNV Molecular Diagnostics / PCR
DICER1-assozierte Tumordisposition DICER1-assozierte Tumordisposition Molecular Diagnostics / PCR
Darmkrebs, adenomatöse Polyposis Darmkrebs, adenomatöse Polyposis Molecular Diagnostics / PCR
Gorlin-Goltz-Syndrom (SUFU, PTCH1 ); SNV, CNV Gorlin-Goltz-Syndrom (SUFU, PTCH1 ); SNV, CNV Molecular Diagnostics / PCR
Hirntumore (APC, BRCA2, CDKN2A, MLH1, MSH2, MSH6, PMS2, POLD1, POLE, PTEN, SUFU, TP53 ); SNV, CNV Hirntumore (APC, BRCA2, CDKN2A, MLH1, MSH2, MSH6, PMS2, POLD1, POLE, PTEN, SUFU, TP53 ); SNV, CNV Molecular Diagnostics / PCR
Infantile Myofibromatose Infantile Myofibromatose Molecular Diagnostics / PCR
Juvenile Polyposis (BMPR1A, SMAD4 ); SNV, CNV Juvenile Polyposis (BMPR1A, SMAD4 ); SNV, CNV Molecular Diagnostics / PCR
Leukämie, familiäre (ANKRD26, CEBPA, ETV6, GATA2, RUNX1 ); SNV, CNV Leukämie, familiäre (ANKRD26, CEBPA, ETV6, GATA2, RUNX1 ); SNV, CNV Molecular Diagnostics / PCR
Li-Fraumeni-Syndrom (TP53 ); SNV, CNV Li-Fraumeni-Syndrom (TP53 ); SNV, CNV Molecular Diagnostics / PCR
Lynch-Syndrom (MLH1, PMS2, MSH2, MSH6, EPCAM ); SNV, CNV Lynch-Syndrom (MLH1, PMS2, MSH2, MSH6, EPCAM ); SNV, CNV Molecular Diagnostics / PCR
Magenkarzinom (diffuses)- Mammakarzinom (lobuläres)- Syndrom (CDH1 , CTNNA1 ); SNV, CNV Magenkarzinom (diffuses)- Mammakarzinom (lobuläres)- Syndrom (CDH1 , CTNNA1 ); SNV, CNV Molecular Diagnostics / PCR
Multiple Endokrine Neoplasie Typ Multiple endokrine Neoplasie Typ Molecular Diagnostics / PCR
Multiple Endokrine Neoplasie Typ 2 Multiple endokrine Neoplasie Typ 2 Molecular Diagnostics / PCR
Neuroblastom (ALK, PHOX2B ); SNV, CNV Neuroblastom (ALK, PHOX2B ); SNV, CNV Molecular Diagnostics / PCR
Neurofibromatose Typ 1 (NF1 ); Neurofibromatose Typ 1 (NF1) Molecular Diagnostics / PCR
Neurofibromatose Typ 2, Schwannomatose (LZTR1, NF2, SMARCB1 ); SNV, CNV Neurofibromatose Typ 2, Schwannomatose (LZTR1, NF2, SMARCB1 ); SNV, CNV Molecular Diagnostics / PCR
Nierentumore, familiäre (FH, FLCN, MET, PTEN, SDHB, SDHC, SDHD, VHL, BAP1, TSC1, TSC2 ); SNV, CNV Nierentumore, familiäre (FH, FLCN, MET, PTEN, SDHB, SDHC, SDHD, VHL, BAP1, TSC1, TSC2 ); SNV, CNV Molecular Diagnostics / PCR
Paragangliom, Phäochromozytom Paragangliom, Phäochromozytom Molecular Diagnostics / PCR
Rhabdoid-Tumor- Dispositionsyndrom (SMARCA4, SMARCB1 ); SNV, CNV Rhabdoid-Tumor- Dispositionsyndrom (SMARCA4, SMARCB1 ); SNV, CNV Molecular Diagnostics / PCR
Tuberöse Sklerose (TSC1, TSC2 ) Tuberöse Sklerose (TSC1, TSC2) Molecular Diagnostics / PCR
Whole Exome Sequencing (WES) Whole Exome Sequencing (WES) Molecular Diagnostics / PCR
(BRCA1, BRCA2, ATM, BARD1, BRIP1, CDH1, CHEK2, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53 ); (BRCA1, BRCA2, ATM, BARD1, BRIP1, CDH1, CHEK2, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53 ); Other
(TruSight Oncology 500 v2) (RET ); (TruSight Oncology 500 v2) (RET ); Other
, ATM , BRCA1, BRCA2, CDKN2A, , ATM , BRCA1, BRCA2, CDKN2A, Other
BRCA1, BRCA2, CHEK2, MLH1, BRCA1, BRCA2, CHEK2, MLH1, Other
MLH1, MSH2, MSH6, PALB2, STK11, TP53 ); SNV, CNV MLH1, MSH2, MSH6, PALB2, STK11, TP53 ); SNV, CNV Other
MSH2, MSH6, PMS2, PALB2, RAD51D, HOXB13- Foundervariante); SNV, CNV MSH2, MSH6, PMS2, PALB2, RAD51D, HOXB13- Foundervariante); SNV, CNV Other
Noonan-Syndrom Basis (PTPN11 ); Noonan-Syndrom Basis (PTPN11 ); Other
Pankreaskarzinom, familiäres (APC Pankreaskarzinom, familiäres (APC Other
Peutz-Jeghers-Syndrom (STK11 ); Peutz-Jeghers-Syndrom (STK11 ); Other
Prostatakarzinom, familiäres (ATM, Prostatakarzinom, familiäres (ATM, Other
SNV, CNV SNV, CNV Other
a Die Proben werden vom Labor ohne vorherige histologische Beurteilung a Die Proben werden vom Labor ohne vorherige histologische Beurteilung Other
bearbeitet und analysiert. bearbeitet und analysiert. Other

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