Source: CURATED ×
| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
T | 0.700 | GeneticVariation | CLINVAR | Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients. | 27279923 | 2016 |
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T | 0.700 | GeneticVariation | CLINVAR | Toward an improved definition of the genetic and tumor spectrum associated with SDH germ-line mutations. | 25394176 | 2015 |
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T | 0.700 | GeneticVariation | CLINVAR | Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing. | 24728327 | 2014 |
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T | 0.700 | GeneticVariation | CLINVAR | Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas. | 24102379 | 2014 |
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T | 0.700 | GeneticVariation | CLINVAR | A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma. | 23666964 | 2013 |
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T | 0.700 | GeneticVariation | CLINVAR | Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. | 23175444 | 2013 |
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T | 0.700 | GeneticVariation | CLINVAR | Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out. | 19351833 | 2009 |