Variant: rs387906677 

    present in Gene: FGFR2
    present in Chromosome: 10
    Position on Chromosome: 121515232
    Alleles of this Variant: A/C

rs387906677 in FGFR2 gene and BENT BONE DYSPLASIA SYNDROME PMID 22387015 2012 Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling.