ClinVar Miner

Submissions for variant NM_020964.3(EPG5):c.3582+12G>C

gnomAD frequency: 0.00001  dbSNP: rs554695413
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002129591 SCV002408185 benign Vici syndrome 2026-01-31 criteria provided, single submitter clinical testing

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