Variant: rs199830292 

    present in Gene: KCNJ5
    present in Chromosome: 11
    Position on Chromosome: 128916630
    Alleles of this Variant: G/C

rs199830292 in KCNJ5 gene and Andersen Syndrome PMID 24574546 2014 A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1.

rs199830292 in KCNJ5 gene and LONG QT SYNDROME 13 PMID 20560207 2010 Identification of a Kir3.4 mutation in congenital long QT syndrome.