ClinVar Miner

Submissions for variant NM_003380.5(VIM):c.720+18C>T

dbSNP: rs7096093
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001767926 SCV002008209 likely benign not provided 2020-09-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002074029 SCV002407190 benign Cataract 30 2024-01-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001767926 SCV005227023 likely benign not provided criteria provided, single submitter not provided

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