BRCA2

Panel	Reviews	Mode of inheritance	Details
Filter panels 23 panels
Green BRCA2 in Bone Marrow Failure Level 2: Haematological disorders Version 1.129 Component of the following Super Panels: Immunological disorders_SuperPanel	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group D1, MIM# 605724
Red BRCA2 in Congenital diaphragmatic hernia Level 2: Dysmorphic and congenital abnormality syndromes Version 1.17	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Fanconi anemia, complementation group D1, MIM# 605724
Green BRCA2 in Chromosome Breakage Disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 1.24	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Fanconi anemia, complementation group D1, MIM# 605724
Green BRCA2 in Incidentalome Version 0.360	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Victorian Clinical Genetics Services Phenotypes Breast-ovarian cancer, familial, 2, MIM#612555 Tags cancer
Green BRCA2 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.357	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Fanconi anemia, complementation group D1 (MIM#605724)
Green BRCA2 in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.132	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green BRCA2 in Radial Ray Abnormalities Level 2: Dysmorphic and congenital abnormality syndromes Version 1.19 Component of the following Super Panels: Limb and Digital Malformations SuperPanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group D1, MIM# 605724
Green BRCA2 in Additional findings_Adult Level 2: Screening Version 1.130	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Breast-ovarian cancer, familial, 2, MIM#612555 Fanconi anaemia, complementation group D1, MIM# 605724
Green BRCA2 in Primary Ovarian Insufficiency_Premature Ovarian Failure Level 3: Gonadal and sex development disorders Level 2: Endocrine disorders Version 0.388	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Fanconi anemia, complementation group D1 MIM#605724 premature ovarian failure
Green BRCA2 in Medulloblastoma Level 2: Cancer Predisposition Version 1.1	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Medulloblastoma, MONDO:0007959 BRCA2-related cancer predisposition, MONDO:0700269 Breast-ovarian cancer, familial, 2, MIM#612555
Red BRCA2 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene BabySeq Category A gene Phenotypes Breast-ovarian cancer, familial, 2 Fanconi anemia, complementation group D1
Green BRCA2 in Incidentalome_PREGEN_DRAFT Version 0.43	1 review	Unknown	Sources NSW Health Pathology Expert Review Green
Green BRCA2 in Growth failure Version 1.83	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group D1, MIM# 605724
Green BRCA2 in Fetal anomalies Version 1.465	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Literature Literature Phenotypes Fanconi anaemia, complementation group D1, MIM# 605724
Green BRCA2 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category C gene BabySeq Category A gene BeginNGS Phenotypes Fanconi anaemia, complementation group D1, MIM# 605724 Tags treatable haematological
Green BRCA2 in Transplant Co-Morbidity Level 2: Screening Version 0.20	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Breast-ovarian cancer, familial, 2, MIM#612555
Green BRCA2 in Sarcoma soft tissue Level 2: Cancer Predisposition Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Soft tissue sarcoma, MONDO:0018078 Sarcoma, MONDO:0005089 BRCA2-related cancer predisposition, MONDO:0700269 Breast-ovarian cancer, familial, 2, MIM#612555
Green BRCA2 in Wilms Tumour Level 2: Cancer Predisposition Version 1.1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Expert list Phenotypes Wilms tumor, MONDO:0006058 Fanconi anemia complementation group D1,MONDO:0011584 Fanconi anemia, complementation group D1, MIM#605724
Green BRCA2 in Pancreatic Cancer Level 2: Cancer Predisposition Version 1.1	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Malignant pancreatic neoplasm, MONDO:0009831 BRCA2-related cancer predisposition, MONDO:0700269 Breast-ovarian cancer, familial, 2, MIM#612555
Green BRCA2 in Prostate Cancer Level 2: Cancer Predisposition Version 1.1	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Prostate cancer, MONDO:0008315 BRCA2-related cancer predisposition, MONDO:0700269 Breast-ovarian cancer, familial, 2, MIM#612555
Green BRCA2 in Ovarian Cancer Level 2: Cancer Predisposition Version 1.1	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Ovarian cancer, MONDO:0008170 BRCA2-related cancer predisposition, MONDO:0700269 Breast-ovarian cancer, familial, 2, MIM#612555
Green BRCA2 in Breast Cancer Level 2: Cancer Predisposition Version 1.1	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Breast cancer, MONDO:0007254 BRCA2-related cancer predisposition, MONDO:0700269 Breast-ovarian cancer, familial, 2, MIM#612555
Amber BRCA2 in Infertility and Recurrent Pregnancy Loss Version 1.50	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Premature ovarian failure

BRCA2

23 panels

Green BRCA2 in Bone Marrow Failure

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Phenotypes

Red BRCA2 in Congenital diaphragmatic hernia

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Phenotypes

Green BRCA2 in Chromosome Breakage Disorders

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Phenotypes

Green BRCA2 in Incidentalome

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Phenotypes

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Green BRCA2 in Microcephaly

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Phenotypes

Green BRCA2 in Cancer Predisposition_Paediatric

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Green BRCA2 in Radial Ray Abnormalities

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Phenotypes

Green BRCA2 in Additional findings_Adult

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Phenotypes

Green BRCA2 in Primary Ovarian Insufficiency_Premature Ovarian Failure

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Phenotypes

Green BRCA2 in Medulloblastoma

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Phenotypes

Red BRCA2 in Additional findings_Paediatric

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Phenotypes

Green BRCA2 in Incidentalome_PREGEN_DRAFT

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Green BRCA2 in Growth failure

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Phenotypes

Green BRCA2 in Fetal anomalies

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Phenotypes

Green BRCA2 in Genomic newborn screening: BabyScreen+

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Phenotypes

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Green BRCA2 in Transplant Co-Morbidity

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Phenotypes

Green BRCA2 in Sarcoma soft tissue

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Phenotypes

Green BRCA2 in Wilms Tumour

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Phenotypes

Green BRCA2 in Pancreatic Cancer

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Green BRCA2 in Prostate Cancer

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Green BRCA2 in Ovarian Cancer

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Phenotypes

Green BRCA2 in Breast Cancer

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Phenotypes

Amber BRCA2 in Infertility and Recurrent Pregnancy Loss

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Phenotypes