Variant: rs1561498701 

    present in Gene: SMN1;SMN2
    present in Chromosome: 5
    Position on Chromosome: 70925150
    Alleles of this Variant: -/GGATTCCG

rs1561498701 in SMN1;SMN2 gene and Absent reflex PMID 24498607 2013 A homozygous double mutation in SMN1: a complicated genetic diagnosis of SMA.

rs1561498701 in SMN1;SMN2 gene and Fasciculation, Tongue PMID 24498607 2013 A homozygous double mutation in SMN1: a complicated genetic diagnosis of SMA.

rs1561498701 in SMN1;SMN2 gene and Generalized hypotonia PMID 24498607 2013 A homozygous double mutation in SMN1: a complicated genetic diagnosis of SMA.

rs1561498701 in SMN1;SMN2 gene and Muscular Atrophy, Spinal, Type II PMID 24498607 2013 A homozygous double mutation in SMN1: a complicated genetic diagnosis of SMA.

rs1561498701 in SMN1;SMN2 gene and Severe muscular hypotonia PMID 24498607 2013 A homozygous double mutation in SMN1: a complicated genetic diagnosis of SMA.