ClinVar Miner

Submissions for variant NM_003380.5(VIM):c.1008+18A>G

gnomAD frequency: 0.00103  dbSNP: rs368836644
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002132207 SCV002406201 benign Cataract 30 2022-07-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718998 SCV005317020 benign not provided criteria provided, single submitter not provided

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