Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer. | 27165003 | 2016 |
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|
A | 0.700 | CausalMutation | CLINVAR | Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer. | 25058500 | 2015 |
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|
A | 0.700 | CausalMutation | CLINVAR | Mutations in BRIP1 confer high risk of ovarian cancer. | 21964575 | 2011 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. | 17033622 | 2006 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia. | 16116424 | 2005 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ. | 16153896 | 2005 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. | 25980754 | 2015 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | A recurrent truncating germline mutation in the BRIP1/FANCJ gene and susceptibility to prostate cancer. | 19127258 | 2009 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease. | 24556621 | 2014 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J. | 16116423 | 2005 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | Hereditary breast cancer and the BRCA1-associated FANCJ/BACH1/BRIP1. | 21345144 | 2011 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. | 22006311 | 2011 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | Evaluation of variants in the CHEK2, BRIP1 and PALB2 genes in an Irish breast cancer cohort. | 19763819 | 2010 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | GeneticVariation | CLINVAR |