ClinVar Miner

Submissions for variant NM_015087.5(SPART):c.180A>G (p.Ser60=)

gnomAD frequency: 0.00001  dbSNP: rs758310379
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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 RCV000942438 SCV001088362 likely benign not provided 2019-08-11 criteria provided, single submitter clinical testing

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