Variant: rs786200925 

    present in Gene: WNT5A
    present in Chromosome: 3
    Position on Chromosome: 55479457
    Alleles of this Variant: C/G

rs786200925 in WNT5A gene and ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 PMID 19918918 2010 WNT5A mutations in patients with autosomal dominant Robinow syndrome.

rs786200925 in WNT5A gene and Robinow Syndrome PMID 19918918 2010 WNT5A mutations in patients with autosomal dominant Robinow syndrome.