RS886041300 KCNH1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Severe intellectual disability
Abnormal facial shape
Seizure
Zimmermann-Laband syndrome 1
Temple-Baraitser syndrome
Intellectual disability
KCNH1-related disorder
Inborn genetic diseases
Severe intellectual disability
Abnormal facial shape
Seizure
Zimmermann-Laband syndrome 1
Temple-Baraitser syndrome
Intellectual disability
Other Variants in KCNH1