ClinVar Miner

Submissions for variant NM_000143.4(FH):c.1237-9_1237-8insCTCTCTCTCTCTCT

dbSNP: rs1553340717
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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 RCV002563318 SCV001702925 likely benign not provided 2024-10-10 criteria provided, single submitter clinical testing

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