Source: CURATED ×
| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
A | 0.700 | CausalMutation | CLINVAR | Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes. | 23551045 | 2013 |
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|
A | 0.700 | CausalMutation | CLINVAR | MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma. | 22452945 | 2012 |
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|
A | 0.700 | CausalMutation | CLINVAR | Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma. | 21685915 | 2011 |