Variant: rs759103701 

    present in Gene: MYCN
    present in Chromosome: 2
    Position on Chromosome: 15945666
    Alleles of this Variant: C/G;T

rs759103701 in MYCN gene and Esophageal atresia with or without tracheoesophageal fistula PMID 15821734 2005 MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.

rs759103701 in MYCN gene and FEINGOLD SYNDROME 1 PMID 15821734 2005 MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.

PMID 18470948 2008 Genotype-phenotype correlations in MYCN-related Feingold syndrome.

rs759103701 in MYCN gene and Short middle phalanx of finger PMID 15821734 2005 MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.

rs759103701 in MYCN gene and Short palpebral fissure PMID 15821734 2005 MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.