ClinVar Miner

Submissions for variant NM_153026.3(PRICKLE1):c.1092A>G (p.Ser364=)

dbSNP: rs2140101756
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002181759 SCV002488793 likely benign Epilepsy, progressive myoclonic, 1B 2020-12-22 criteria provided, single submitter clinical testing

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