Variant: rs17036328 

    present in Gene: PPARG
    present in Chromosome: 3
    Position on Chromosome: 12348985
    Alleles of this Variant: T/C

rs17036328 in PPARG gene and Body mass index PMID 27416945 2016 Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci.

rs17036328 in PPARG gene and Insulin Sensitivity Measurement PMID 27416945 2016 Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci.

rs17036328 in PPARG 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.