ClinVar Miner

Submissions for variant NM_000430.4(PAFAH1B1):c.171T>G (p.Ser57=)

dbSNP: rs765448987
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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 RCV001942077 SCV002229522 likely benign not provided 2021-11-25 criteria provided, single submitter clinical testing

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