|
Malignant neoplasm of breast
|
|
0.710 |
GeneticVariation
|
BEFREE |
PALB2 c.2257C>T truncating variant is a Greek founder and is associated with high breast cancer risk.
|
31089269 |
2019 |
|
Malignant neoplasm of breast
|
|
0.710 |
CausalMutation
|
CLINVAR |
Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer.
|
21618343 |
2011 |
|
Malignant neoplasm of breast
|
|
0.710 |
CausalMutation
|
CLINVAR |
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
|
17200671 |
2007 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Frequency of pathogenic germline mutation in CHEK2, PALB2, MRE11, and RAD50 in patients at high risk for hereditary breast cancer.
|
27783279 |
2017 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Revisiting breast cancer patients who previously tested negative for BRCA mutations using a 12-gene panel.
|
27798748 |
2017 |
|
Hereditary Breast and Ovarian Cancer Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
Frequency of pathogenic germline mutation in CHEK2, PALB2, MRE11, and RAD50 in patients at high risk for hereditary breast cancer.
|
27783279 |
2017 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer.
|
25452441 |
2015 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Breast-cancer risk in families with mutations in PALB2.
|
25099575 |
2014 |
|
Hereditary Breast and Ovarian Cancer Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer.
|
21618343 |
2011 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer.
|
21618343 |
2011 |
|
Hereditary Breast and Ovarian Cancer Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
A PALB2 germline mutation associated with hereditary breast cancer in Italy.
|
19763884 |
2010 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
A PALB2 germline mutation associated with hereditary breast cancer in Italy.
|
19763884 |
2010 |
|
Hereditary Breast and Ovarian Cancer Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene.
|
19264984 |
2009 |
|
Hereditary Breast and Ovarian Cancer Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
|
17200671 |
2007 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
|
17200671 |
2007 |
|
Breast Carcinoma
|
|
0.010 |
GeneticVariation
|
BEFREE |
PALB2 c.2257C>T truncating variant is a Greek founder and is associated with high breast cancer risk.
|
31089269 |
2019 |