Variant: rs587781912 

    present in Gene: PTEN;KLLN
    present in Chromosome: 10
    Position on Chromosome: 87864519
    Alleles of this Variant: AA/-

rs587781912 in PTEN;KLLN gene and Neoplastic Syndromes, Hereditary PMID 20223021 2006 Germline PTEN mutations are rare and highly penetrant.

rs587781912 in PTEN;KLLN gene and PTEN Hamartoma Tumor Syndrome PMID 20223021 2006 Germline PTEN mutations are rare and highly penetrant.