Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
Neoplastic Syndromes, Hereditary
|
0.700 | CausalMutation | CLINVAR | Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome. | 26607058 | 2015 | |||||
Neoplastic Syndromes, Hereditary
|
0.700 | CausalMutation | CLINVAR | Frequency and spectrum of cancers in the Peutz-Jeghers syndrome. | 16707622 | 2006 | |||||
Neoplastic Syndromes, Hereditary
|
0.700 | CausalMutation | CLINVAR | An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus. | 17026623 | 2006 | |||||
Neoplastic Syndromes, Hereditary
|
0.700 | CausalMutation | CLINVAR | High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome. | 16287113 | 2005 | |||||
Neoplastic Syndromes, Hereditary
|
0.700 | CausalMutation | CLINVAR | Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients. | 12372054 | 2002 | |||||
Neoplastic Syndromes, Hereditary
|
0.700 | CausalMutation | CLINVAR | Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma. | 11389158 | 2001 | |||||
Peutz-Jeghers Syndrome
|
0.700 | CausalMutation | CLINVAR |