ClinVar Miner

Submissions for variant NM_000430.4(PAFAH1B1):c.1003-4del

dbSNP: rs2544121392
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002815457 SCV003207281 benign not provided 2022-06-02 criteria provided, single submitter clinical testing

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