RS58173258 CACNA1H
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What This Variant Does
"[OMIM:?]
Associated Conditions
Epilepsy
idiopathic generalized
susceptibility to
6
Hyperaldosteronism
familial
type IV
Idiopathic generalized epilepsy
childhood absence
CACNA1H-related disorder
Epilepsy
idiopathic generalized
susceptibility to
6
Hyperaldosteronism
Other Variants in CACNA1H