DisGeNET - a database of gene-disease associations

Malignant neoplasm of breast, C0006142

Gene: BRCA1 ×

Source: CURATED ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs1450793674

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs397507232

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs397508869

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs397508893

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs397508994

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs397509022

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs397509034

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs397509037

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs397509218

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs397509238

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs397509246

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs397509275

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs41293447

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs45553935

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs55688530

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs55815649

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs56046357

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs56195342

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs56214134

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs587782190

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs769650474

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs786202389

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs786203152

BRCA1 ; NBR2

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs80356860

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017

dbSNP:

rs80356865

BRCA1

0.700

GeneticVariation

UNIPROT

Suggestion of BRCA1 c.5339T>C (p.L1780P) variant confer from 'unknown significance' to 'Likely pathogenic' based on clinical evidence in Korea.

28364669

2017