ClinVar Miner

Submissions for variant NM_000097.7(CPOX):c.878C>T (p.Ala293Val)

gnomAD frequency: 0.00020  dbSNP: rs140475004
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 RCV000805538 SCV000945496 benign not provided 2024-08-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000805538 SCV005189705 uncertain significance not provided criteria provided, single submitter not provided

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