ClinVar Miner

Submissions for variant NM_058179.4(PSAT1):c.741-18_741-17delinsAC

dbSNP: rs2118681211
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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 RCV001968277 SCV002237555 likely benign Neu-Laxova syndrome 2 2024-03-06 criteria provided, single submitter clinical testing

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