Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
Neoplasms
|
0.710 | GeneticVariation | CLINVAR | Prospective enterprise-level molecular genotyping of a cohort of cancer patients. | 25157968 | 2014 | |||||
Thyroid Neoplasm
|
0.710 | CausalMutation | CLINVAR | Selumetinib-enhanced radioiodine uptake in advanced thyroid cancer. | 23406027 | 2013 | |||||
Thyroid Neoplasm
|
0.710 | CausalMutation | CLINVAR | Selumetinib-enhanced radioiodine uptake in advanced thyroid cancer. | 23406027 | 2013 | |||||
Organoid Nevus Phakomatosis
|
0.710 | GeneticVariation | BEFREE | Mosaicism for HRAS c.37G>C and KRAS c.35G>A mutations was found in two individuals with Schimmelpenning syndrome. | 22683711 | 2012 | |||||
Thyroid Neoplasm
|
0.710 | CausalMutation | CLINVAR | Phase II trial of sorafenib in metastatic thyroid cancer. | 19255327 | 2009 | |||||
Thyroid Neoplasm
|
0.710 | CausalMutation | CLINVAR | Phase II trial of sorafenib in metastatic thyroid cancer. | 19255327 | 2009 | |||||
Thyroid Neoplasm
|
0.710 | CausalMutation | CLINVAR | Beneficial effects of sorafenib on tumor progression, but not on radioiodine uptake, in patients with differentiated thyroid carcinoma. | 19773371 | 2009 | |||||
Thyroid Neoplasm
|
0.710 | CausalMutation | CLINVAR | Beneficial effects of sorafenib on tumor progression, but not on radioiodine uptake, in patients with differentiated thyroid carcinoma. | 19773371 | 2009 | |||||
Thyroid Neoplasm
|
0.710 | CausalMutation | CLINVAR | Hyperactive Ras in developmental disorders and cancer. | 17384584 | 2007 | |||||
Thyroid Neoplasm
|
0.710 | CausalMutation | CLINVAR | Hyperactive Ras in developmental disorders and cancer. | 17384584 | 2007 | |||||
Organoid Nevus Phakomatosis
|
0.710 | CausalMutation | CLINVAR | ||||||||
Organoid Nevus Phakomatosis
|
0.710 | CausalMutation | CLINVAR | ||||||||
Noonan Syndrome
|
0.700 | CausalMutation | CLINVAR | ClinGen's RASopathy Expert Panel consensus methods for variant interpretation. | 29493581 | 2018 | |||||
Gastric Adenocarcinoma
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Squamous cell carcinoma of skin
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Multiple Myeloma
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Mammary Neoplasms
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Adenocarcinoma of lung (disorder)
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Colorectal Neoplasms
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Cutaneous Melanoma
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Liver carcinoma
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Adenocarcinoma of lung (disorder)
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Uterine Cervical Neoplasm
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Chronic Lymphocytic Leukemia
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 | |||||
Colorectal Neoplasms
|
0.700 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 |