ClinVar Miner

Submissions for variant NM_058179.4(PSAT1):c.870-16T>C

gnomAD frequency: 0.00001  dbSNP: rs746255855
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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 RCV002130816 SCV002441849 likely benign Neu-Laxova syndrome 2 2022-07-26 criteria provided, single submitter clinical testing

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