Variant: rs104893827 

    present in Gene: VHL
    present in Chromosome: 3
    Position on Chromosome: 10142035
    Alleles of this Variant: T/A;C

rs104893827 in VHL gene and Pheochromocytoma PMID 24319509 2013 Canadian guideline on genetic screening for hereditary renal cell cancers.

PMID 24893135 2014 Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.

PMID 24493721 2014 American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.