ClinVar Miner

Submissions for variant NM_003380.5(VIM):c.-22G>C

gnomAD frequency: 0.34400  dbSNP: rs3758410
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001692920 SCV001909576 benign not provided 2018-06-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243416 SCV002514470 benign Cataract 30 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001692920 SCV005317014 benign not provided criteria provided, single submitter not provided

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