Variant: rs267607040 

    present in Gene: SETBP1
    present in Chromosome: 18
    Position on Chromosome: 44951948
    Alleles of this Variant: G/A

rs267607040 in SETBP1 gene and Leukemia, Myelocytic, Acute PMID 23648668 2013 SETBP1 mutation analysis in 944 patients with MDS and AML.

PMID 23889083 2013 Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.

rs267607040 in SETBP1 gene and MYELODYSPLASTIC SYNDROME PMID 23648668 2013 SETBP1 mutation analysis in 944 patients with MDS and AML.

PMID 23889083 2013 Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.

rs267607040 in SETBP1 gene and Myeloid Leukemia, Chronic PMID 24976289 2014 Managing children with chronic myeloid leukaemia (CML): recommendations for the management of CML in children and young people up to the age of 18 years.

PMID 23222956 2013 Recurrent SETBP1 mutations in atypical chronic myeloid leukemia.

rs267607040 in SETBP1 gene and Schinzel-Giedion syndrome PMID 20436468 2010 De novo mutations of SETBP1 cause Schinzel-Giedion syndrome.