ClinVar Miner

Submissions for variant NM_000143.4(FH):c.378+15G>A

gnomAD frequency: 0.00001  dbSNP: rs748766342
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 RCV003015242 SCV002387616 likely benign not provided 2024-11-03 criteria provided, single submitter clinical testing

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