Variant: rs786205271 

    present in Gene: SCN5A
    present in Chromosome: 3
    Position on Chromosome: 38551159
    Alleles of this Variant: G/A;C

rs786205271 in SCN5A gene and Arthrogryposis PMID 31680123 2020 The genomic and clinical landscape of fetal akinesia.

rs786205271 in SCN5A gene and Early severe fetal akinesia sequence PMID 31680123 2020 The genomic and clinical landscape of fetal akinesia.