Variant: rs387906651 

    present in Gene: LOC100506321;MAX
    present in Chromosome: 14
    Position on Chromosome: 65093782
    Alleles of this Variant: G/A

rs387906651 in LOC100506321;MAX gene and Hereditary Paraganglioma-Pheochromocytoma Syndrome PMID 21685915 2011 Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.

PMID 22452945 2012 MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma.

PMID 27838885 2017 Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX Mutation.

rs387906651 in LOC100506321;MAX gene and Neoplastic Syndromes, Hereditary PMID 25525159 2015 RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.

PMID 27838885 2017 Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX Mutation.

PMID 22452945 2012 MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma.

PMID 21685915 2011 Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.