ClinVar Miner

Submissions for variant NM_058179.4(PSAT1):c.741-7A>G

dbSNP: rs747801091
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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 RCV002079486 SCV002429728 likely benign Neu-Laxova syndrome 2 2021-11-28 criteria provided, single submitter clinical testing

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