ClinVar Miner

Submissions for variant NM_000143.4(FH):c.904+14T>C

dbSNP: rs2527322670
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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 RCV003543494 SCV004247230 likely benign not provided 2023-11-05 criteria provided, single submitter clinical testing

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