ClinVar Miner

Submissions for variant NM_015192.4(PLCB1):c.2625C>G (p.Pro875=)

dbSNP: rs1600302170
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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 RCV001488113 SCV001692619 likely benign Developmental and epileptic encephalopathy, 12 2018-11-14 criteria provided, single submitter clinical testing

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