RS121912512 KCNH2

Health Risk Chr 7:150950311
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What This Variant Does
"Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neo...
Associated Conditions
Long QT syndrome 2
Congenital long QT syndrome
Long QT syndrome
Cardiovascular phenotype
Cardiac arrhythmia
Long QT syndrome 2
Congenital long QT syndrome
Long QT syndrome
Cardiovascular phenotype
Cardiac arrhythmia
Other Variants in KCNH2
rs121912504 rs121912505 rs28928904 rs121912506 rs1554426258 rs121912507 rs121912508 rs9333649 rs28928905 rs121912509
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