rs201743423, MAX

N. diseases: 1
Disease: Pheochromocytoma ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.700 GeneticVariation UNIPROT Functional and in silico assessment of MAX variants of unknown significance. 26070438 2015
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.700 GeneticVariation UNIPROT American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers. 24493721 2014
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.700 GeneticVariation UNIPROT Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. 24893135 2014
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.700 GeneticVariation UNIPROT Canadian guideline on genetic screening for hereditary renal cell cancers. 24319509 2013
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.700 GeneticVariation UNIPROT MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma. 22452945 2012
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.700 GeneticVariation UNIPROT Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma. 21685915 2011