Variant: rs121909083 

    present in Gene: ROR2
    present in Chromosome: 9
    Position on Chromosome: 91724990
    Alleles of this Variant: G/A

rs121909083 in ROR2 gene and Robinow syndrome, autosomal recessive PMID 10932186 2000 Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.