Variant: rs1554919471 

    present in Gene: KCNQ1
    present in Chromosome: 11
    Position on Chromosome: 2768861
    Alleles of this Variant: G/-

rs1554919471 in KCNQ1 gene and Congenital sensorineural hearing loss PMID 29372044 2018 Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome.

rs1554919471 in KCNQ1 gene and Jervell And Lange-Nielsen Syndrome 1 PMID 29372044 2018 Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome.

rs1554919471 in KCNQ1 gene and Prolonged QT interval PMID 29372044 2018 Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome.

rs1554919471 in KCNQ1 gene and Syncope PMID 29372044 2018 Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome.