ClinVar Miner

Submissions for variant NM_000143.4(FH):c.268-16T>G

dbSNP: rs2527335378
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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 RCV003574681 SCV004334131 likely benign not provided 2023-10-28 criteria provided, single submitter clinical testing

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