ClinVar Miner

Submissions for variant NM_024513.4(FYCO1):c.1677G>A (p.Pro559=)

gnomAD frequency: 0.00002  dbSNP: rs928579946
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002115491 SCV002393969 likely benign Cataract 18 2022-07-19 criteria provided, single submitter clinical testing

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