ClinVar Miner

Submissions for variant NM_024513.4(FYCO1):c.1815G>T (p.Val605=)

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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 RCV005169709 SCV005802901 likely benign Cataract 18 2024-10-16 criteria provided, single submitter clinical testing

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