Source: CURATED ×
| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
A | 0.700 | CausalMutation | CLINVAR | Pheochromocytoma and paraganglioma syndromes: genetics and management update. | 24523625 | 2014 |
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|
A | 0.700 | CausalMutation | CLINVAR | Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. | 16317055 | 2006 |
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|
A | 0.700 | CausalMutation | CLINVAR | Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma. | 16405730 | 2006 |