Variant: rs6782299 

    present in Gene: LOC101928882;CCDC39
    present in Chromosome: 3
    Position on Chromosome: 180832914
    Alleles of this Variant: G/T

rs6782299 in LOC101928882;CCDC39 gene and Leukemia, Myelocytic, Acute PMID 27903959 2017 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

rs6782299 in LOC101928882;CCDC39 gene and Schizophrenia PMID 19571811 2009 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.