Variant: rs1554890324 

    present in Gene: KLLN;PTEN
    present in Chromosome: 10
    Position on Chromosome: 87864470
    Alleles of this Variant: A/G

rs1554890324 in KLLN;PTEN gene and Hamartoma Syndrome, Multiple PMID 21194675 2011 A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands.

PMID 24498881 2014 A novel deleterious PTEN mutation in a patient with early-onset bilateral breast cancer.

PMID 22503188 2012 Challenges in the management of a patient with Cowden syndrome: case report and literature review.