Variant: rs200052869 

    present in Gene: PRDM16
    present in Chromosome: 1
    Position on Chromosome: 3402925
    Alleles of this Variant: G/A

rs200052869 in PRDM16 gene and LEFT VENTRICULAR NONCOMPACTION 8 PMID 23768516 2013 Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.