Variant: rs104893646 

    present in Gene: MYCN
    present in Chromosome: 2
    Position on Chromosome: 15945880
    Alleles of this Variant: G/A

rs104893646 in MYCN gene and FEINGOLD SYNDROME 1 PMID 18470948 2008 Genotype-phenotype correlations in MYCN-related Feingold syndrome.

PMID 15821734 2005 MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.

PMID 16906565 2006 Expanding the clinical spectrum of MYCN-related Feingold syndrome.