Breast-ovarian Cancer, Familial, Susceptibility To, 2; Brovca2

Clinical Features

Phenotypes and symptoms related to Breast-ovarian Cancer, Familial, Susceptibility To, 2; Brovca2

  • Neoplasm
  • Breast carcinoma
  • Ovarian neoplasm

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.


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Breast-ovarian Cancer, Familial, Susceptibility To, 2; Brovca2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
BRCA2.

By Molecular Diagnostic Laboratory University of Alberta (Canada).

BRCA2
Specificity
100 %
Genes
100 %
BRCA1 & BRCA2 Seq and Del/Dup Analysis.

By Baylor Miraca Genetics Laboratories (United States).

BRCA1, BRCA2
Specificity
50 %
Genes
100 %
Hereditary High Risk Breast Cancer Panel.

By Baylor Miraca Genetics Laboratories (United States).

BRCA1, BRCA2, STK11, TP53, CDH1, PALB2, PTEN
Specificity
15 %
Genes
100 %
BRCA1 & BRCA2 Seq and Del/Dup Analysis.

By Baylor Miraca Genetics Laboratories (United States).

BRCA1, BRCA2
Specificity
50 %
Genes
100 %
Hereditary High Risk Breast Cancer Panel.

By Baylor Miraca Genetics Laboratories (United States).

BRCA1, BRCA2, STK11, TP53, CDH1, PALB2, PTEN
Specificity
15 %
Genes
100 %
Hereditary Melanoma Panel.

By Baylor Miraca Genetics Laboratories (United States).

BRCA2, TP53, CDK4, CDKN2A
Specificity
25 %
Genes
100 %
Hereditary Prostate Cancer Panel.

By Baylor Miraca Genetics Laboratories (United States).

BRCA1, BRCA2, TP53, NBN
Specificity
25 %
Genes
100 %
Hereditary Pancreatic Cancer Panel.

By Baylor Miraca Genetics Laboratories (United States).

BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TP53, CDK4, CDKN2A, PALB2, APC, SMAD4, MLH1, MSH2, MSH6, ATM, PMS2, RAD50
Specificity
6 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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