rs759514392

This variant is located in the CACNA1S gene.

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ClinVar annotation

Uncertain Significance★★★☆
4 submitters2 publications

CACNA1S-related disorder; Hypokalemic periodic paralysis, type 1;Malignant hyperthermia, susceptibility to, 5; Malignant hyperthermia, susceptibility to, 5; Inborn genetic diseases

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About CACNA1S

This gene encodes one of the five subunits of the slowly inactivating L-type voltage-dependent calcium channel in skeletal muscle cells. Mutations in this gene have been associated with hypokalemic periodic paralysis, thyrotoxic periodic paralysis and malignant hyperthermia susceptibility. [provided by RefSeq, Jul 2008]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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