ClinVar Miner

Submissions for variant NM_024513.4(FYCO1):c.108G>A (p.Thr36=)

gnomAD frequency: 0.00001  dbSNP: rs558777911
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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 RCV001480465 SCV001684781 likely benign Cataract 18 2020-12-03 criteria provided, single submitter clinical testing

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