RS397508112 KCNQ1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital long QT syndrome
Jervell and Lange-Nielsen syndrome
Rare genetic deafness
Long QT syndrome 1
Cardiovascular phenotype
Long QT syndrome
KCNQ1-related disorder
Congenital long QT syndrome
Jervell and Lange-Nielsen syndrome
Rare genetic deafness
Long QT syndrome 1
Cardiovascular phenotype
Long QT syndrome
KCNQ1-related disorder
Other Variants in KCNQ1