ClinVar Miner

Submissions for variant NM_004230.4(S1PR2):c.216G>C (p.Leu72=)

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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 RCV005075181 SCV005702114 likely benign not provided 2024-08-31 criteria provided, single submitter clinical testing

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