Variant: rs375218091 

    present in Gene: RAPSN
    present in Chromosome: 11
    Position on Chromosome: 47448071
    Alleles of this Variant: C/A;T

rs375218091 in RAPSN gene and Arthrogryposis PMID 31680123 2020 The genomic and clinical landscape of fetal akinesia.

rs375218091 in RAPSN gene and Early severe fetal akinesia sequence PMID 31680123 2020 The genomic and clinical landscape of fetal akinesia.