ClinVar Miner

Submissions for variant NM_005876.5(SPEG):c.3645C>G (p.Pro1215=)

dbSNP: rs374311978
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002178992 SCV002479289 likely benign not provided 2021-08-06 criteria provided, single submitter clinical testing

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