ClinVar Miner

Submissions for variant NM_014000.3(VCL):c.168+7G>T

gnomAD frequency: 0.00003  dbSNP: rs780959726
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001493025 SCV001697647 likely benign Dilated cardiomyopathy 1W 2022-08-28 criteria provided, single submitter clinical testing

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