Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201743423
rs201743423
MAX
0.700 GeneticVariation UNIPROT Functional and in silico assessment of MAX variants of unknown significance. 26070438

2015
dbSNP: rs201743423
rs201743423
MAX
0.700 GeneticVariation UNIPROT American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers. 24493721

2014
dbSNP: rs201743423
rs201743423
MAX
0.700 GeneticVariation UNIPROT Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. 24893135

2014
dbSNP: rs201743423
rs201743423
MAX
0.700 GeneticVariation UNIPROT Canadian guideline on genetic screening for hereditary renal cell cancers. 24319509

2013
dbSNP: rs201743423
rs201743423
MAX
0.700 GeneticVariation UNIPROT MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma. 22452945

2012
dbSNP: rs201743423
rs201743423
MAX
0.700 GeneticVariation UNIPROT Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma. 21685915

2011