Variant: rs121917856 

    present in Gene: MIR3131;IHH
    present in Chromosome: 2
    Position on Chromosome: 219060331
    Alleles of this Variant: G/A

rs121917856 in MIR3131;IHH gene and Acrocapitofemoral Dysplasia PMID 12632327 2003 Homozygous mutations in IHH cause acrocapitofemoral dysplasia, an autosomal recessive disorder with cone-shaped epiphyses in hands and hips.