rs80359671, BRCA2

N. diseases: 4
Disease: Neoplastic Syndromes, Hereditary ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR Oestrogen receptor status, treatment and breast cancer prognosis in Icelandic BRCA2 mutation carriers. 27537391 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR Tumour diploidy and survival in breast cancer patients with BRCA2 mutations. 23857704 2013
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR Population-based study of changing breast cancer risk in Icelandic BRCA2 mutation carriers, 1920-2000. 16418514 2006
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR The Icelandic founder mutation BRCA2 999del5: analysis of expression. 15217494 2004
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR Study of a single BRCA2 mutation with high carrier frequency in a small population. 9150155 1997
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes. 8673089 1996
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. 8589730 1996