Variant: rs267607026 

    present in Gene: RUNX1;LOC112267915
    present in Chromosome: 21
    Position on Chromosome: 34880598
    Alleles of this Variant: G/T

rs267607026 in RUNX1;LOC112267915 gene and Platelet Disorder, Familial, with Associated Myeloid Malignancy PMID 19357396 2009 High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder.

PMID 27112265 2016 Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.