ClinVar Miner

Submissions for variant NM_000069.3(CACNA1S):c.1830A>G (p.Val610=)

dbSNP: rs1479771505
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001461415 SCV001665316 likely benign Hypokalemic periodic paralysis, type 1; Malignant hyperthermia, susceptibility to, 5 2023-08-27 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004007079 SCV004842643 likely benign Malignant hyperthermia, susceptibility to, 5 2023-12-13 criteria provided, single submitter clinical testing

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